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  • 2005-2009  (8)
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  • Organic Chemistry  (4,565)
  • 11.10.Ef Lagrangian and Hamiltonian approach
  • ddc:620
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  • 1
    Publication Date: 2016-06-09
    Description: In this paper we revisit the a priori turbulent flame speed tabulation (TFST) technique for a given parameter space within the region of flamelet combustion-regimes. It can be used as a subgrid-scale (SGS) model in Large Eddy Simulation (LES). In a first step, stationary laminar flamelets are computed and stored over the progress variable following the ideas of flamelet generated manifolds (FGM). In a second step, the incompressible one-dimensional Navier-Stokes equations supplemented by the equation for the progress variable are solved on a grid that resolves all turbulent scales. Additionally, turbulent transport is implemented via the linear eddy model (LEM). The turbulent flame structures are solved until a statistically stationary mean value of the turbulent flame speed has been reached. The results are stored in a table that could be used by large scale premixed combustion models, e.g. front tracking schemes. First results are compared quantitatively with direct numerical simulations (DNS) taken from literature. Then it is illustrated in one example how the new method could help to fix constants in algebraic models for turbulent flame speeds. Further it is shown how the technique can be extended to incorporate turbulent strain effects. Finally we investigate the effect of the use of detailed and tabulated chemistry under unsteady conditions.
    Keywords: ddc:620
    Language: English
    Type: reportzib , doc-type:preprint
    Format: application/pdf
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  • 2
    Publication Date: 2016-06-09
    Description: A world-wide used program for the simulation of fire-induced flows is the Fire Dynamics Simulator (FDS) which originally was developed for a purely serial execution on single-processor computing systems. Due to steadily increasing problem sizes and accuracy requirements as well as restrictions in storage capacity and computing power on single-processor systems, the efficient simulation of the considered fire scenarios can only be achieved on modern high-performance systems based on multi-processor architectures. The transition to those systems requires the elaborate parallelization of the underlying numerical methods which must guarantee the same result for a given problem as the corresponding serial execution. Unfortunately, one fundamental serial serial solver of FDS, the pressure solver, only possesses a low degree of inherent parallelizm. Its current parallelization may cause additional numerical errors, casually leading to significant losses of accuracy or even numerical instabilities. In order to ensure that the parallelization errors are limited by the leading error of the numerical scheme such that second order convergence for the whole method can be acchieved, optimized parallelization concepts must be designed. With respect to these considerations this articles gives an overview of the current parallel pressure solver as well as the problems related to it and presents an alternative method, SCARC, to overcome the existing complicacies. Part I explains the theory, concept and implementation of this new strategy, whereas Part II describes a series of validation and verification tests to proof its correctness.
    Keywords: ddc:620
    Language: English
    Type: reportzib , doc-type:preprint
    Format: application/pdf
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  • 3
    Publication Date: 2016-06-09
    Description: Because CFD programs, like FDS, generally consist of a large number of different components representing the variety of participating numerical algorithms and chemical / physical processes, it is nearly impossible to verify such codes in their entirety, for example with comparisons of fire tests. Instead, a careful verification and validation with respect to the underlying mathematical conditions and applied numerical schemes is indispensable. In particular, error cancelations between single program components can only be detected by such detailed component-level tests. In part I of this article series a conceptual deficiency of the FDS program package with regard to multi-mesh computations was illustrated and an alternative domain decomposition strategy FDS-ScaRC was introduced. In this second part we will present the structure of a comprehensive test concept and the needs for a more mathematically and numerically orientated test procedure that is much more suited for a reliable evaluation than only a simple visual comparison of the numerical results with experimental fire tests. After a general introduction of our test concept we will demonstrate the high potential of the new FDS-\scarc{} technique compared to the FDS-FFT technique which is used in the FDS program package as yet. Based on this concept, we will present a comprehensive set of analytical and numerical test results.
    Keywords: ddc:620
    Language: English
    Type: reportzib , doc-type:preprint
    Format: application/pdf
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  • 4
    Publication Date: 2016-06-09
    Description: In this paper we propose a technique for a priori turbulent flame speed tabulation (TFST) for a given parameter space in standard combustion-regime diagrams. It can be used as a subgrid-scale (SGS) model in Large Eddy Simulation (LES). In a first step, stationary laminar flamelets are computed and stored over the progress variable following the ideas of flamelet generated manifolds (FGM). In a second step, the incompressible one-dimensional Navier-Stokes equations supplemented by the equation for the progress variable are solved on a grid that resolves all turbulent scales. Additionally, turbulent transport is implemented via the linear eddy model (LEM). The turbulent flame structures are solved until a statistically stationary mean value of the turbulent flame speed has been reached. The results are stored in a table that could be used by large scale premixed combustion models, e.g. front tracking schemes. Results are compared to an algebraic model and to direct numerical simulations (DNS).
    Keywords: ddc:620
    Language: English
    Type: reportzib , doc-type:preprint
    Format: application/pdf
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  • 5
    Publication Date: 2016-06-09
    Description: The influence of thermal stratification on autoignition at constant volume and high pressure is investigated under turbulent conditions using the one-dimensional Linear-Eddy Model (LEM) and detailed hydrogen/air chemistry. Results are presented for the influence of initial temperature inhomogeneities on the heat release rate and the relative importance of diffusion and chemical reactions. The predicted heat release rates are compared with heat release rates of Chen et al. and Hawkes et al. obtained by two-dimensional Direct Numerical Simulations (DNS). Using the definition of Chen et al. for the displacement speed of the H2 mass fraction tracked at the location of maximum heat release, and a comparison of budget terms, different combustion modes including ignition front propagation and deflagration waves are identified and the results are compared to the DNS data. The LEM approach shows qualitatively and quantitatively reasonable agreement with the DNS data over the whole range of investigated temperature fluctuations. The results presented in this work suggest that LEM is a potential candidate as a sub-model for CFD calculations of HCCI engines.
    Keywords: ddc:620
    Language: English
    Type: reportzib , doc-type:preprint
    Format: application/pdf
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  • 6
    ISSN: 1434-601X
    Keywords: 11.10.Ef Lagrangian and Hamiltonian approach ; 13.75.Gx Pion-baryon interactions ; 36.10.-k Exotic atoms and molecules (containing mesons, muons, and other unusual particles) ; 26.65.+t Solar neutrinos
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract. Within the Nuclear Nambu-Jona-Lasinio model of light nuclei (the NNJL model), describing strong low-energy nuclear interactions, we compute the width of the energy level of the ground state of pionic deuterium. The theoretical value fits well the experimental data. Using the cross-sections for the reactions νe + d → p + p + e- and νe + d → p + n + νe, computed in the NNJL model, and the experimental values of the events of these reactions, detected by the SNO Collaboration, we compute the boron neutrino fluxes. The theoretical values agree well with the experimental data and the theoretical predictions within the Standard Solar Model by Bahcall. We argue the applicability of the constraints on the astrophysical factor for the solar proton burning, imposed by helioseismology, to the width of the energy level of the ground state of pionic deuterium. We show that the experimental data on the width satisfy these constraints. This testifies an indirect measurement of the recommended value of the astrophysical factor for the solar proton burning in terrestrial laboratories in terms of the width of the energy level of the ground state of pionic deuterium.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1434-601X
    Keywords: 11.10.Ef Lagrangian and Hamiltonian approach ; 11.55.Ds Exact S matrices ; 13.75.Gx Pion-baryon interactions ; 36.10.-k Exotic atoms and molecules (containing mesons, muons, and other unusual particles)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract. We study kaonic deuterium, the bound K-d state AK d. Within a quantum field-theoretic and relativistic covariant approach we derive the energy level displacement of the ground state of kaonic deuterium in terms of the amplitude of K-d scattering for arbitrary relative momenta. Near threshold our formula reduces to the well-known DGBT formula. The S-wave amplitude of K-d scattering near threshold is defined by the resonances Λ(1405), Σ(1750) and a smooth elastic background, and the inelastic channels K-d → NY and K-d → NYπ, where Y = Σ±,Σ{0} and Λ{0}, where the final-state interactions play an important role. The Ericson-Weise formula for the S-wave scattering length of K-d scattering is derived. The total width of the energy level of the ground state of kaonic deuterium is estimated using the theoretical predictions of the partial widths of the two-body decays AKd → NY and experimental data on the rates of the NY pair production in the reactions K-d → NY. We obtain Γ{1s} = (630±100)eV. For the shift of the energy level of the ground state of kaonic deuterium we predict ε{1s} = (325±60)eV.
    Type of Medium: Electronic Resource
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  • 8
    Publication Date: 2022-07-19
    Description: In der Arbeit wird die computergestützte Planung von chirurgisch gesetzten Knochenfrakturen bzw. Knochenschnitten (sogenannten Osteotomien) an dreidimensionalen, computergrafischen Schädelmodellen, sowie die Umpositionierung separierter knöcherner Segmente im Kontext der rekonstruktiven MKG-Chirurgie behandelt. Durch die 3D Modellierung und Visualisierung anatomischer Strukturen, sowie der 3D Osteotomie- und Umstellungsplanung unter Einbeziehung der resultierenden Weichgewebedeformation wird den Chirurgen ein Werkzeug an die Hand gegeben, mit dem eine Therapieplanung am Computer durchgeführt und diese in Hinblick auf Funktion und Ästhetik bewertet werden kann. Unterschiedliche Strategien können dabei erprobt und in ihrer Auswirkung erfasst werden. Dazu wird ein methodischer Ansatz vorgestellt, der zum einen die chirurgische Planung im Vergleich zu existierenden Ansätzen deutlich verbessert und zum anderen eine robuste Weichgewebeprognose, durch den Einsatz geeigneter Planungsmodelle und eines physikalisch basierten Weichgewebemodells unter Nutzung numerischer Lösungsverfahren in die Planung integriert. Die Visualisierung der Planungsergebnisse erlaubt sowohl eine anschauliche und überzeugende, präoperative Patientenaufklärung, als auch die Demonstration möglicher Vorgehensweisen und deren Auswirkungen für die chirurgische Ausbildung. Ferner ergänzen die Planungsdaten die Falldokumentation und liefern einen Beitrag zur Qualitätssicherung. Die Arbeit ist in sieben Kapitel gegliedert und wie folgt strukturiert: Zuerst wird die medizinische Aufgabenstellung bei der chirurgischen Rekonstruktion von Knochenfehlbildungen und -fehlstellungen in der kraniofazialen Chirurgie sowie die daraus resultierenden Anforderungen an die Therapieplanung beschrieben. Anschließend folgt ein umfassender Überblick über entsprechende Vorarbeiten zur computergestützten Planung knochenverlagernder Operationen und eine kritische Bestandsaufnahme der noch vorhandenen Defizite. Nach der Vorstellung des eigenen Planungsansatzes wird die Generierung individueller, qualitativ hochwertiger 3D Planungsmodelle aus tomografischen Bilddaten beschrieben, die den Anforderungen an eine intuitive, 3D Planung von Umstellungsosteotomien entsprechen und eine Simulation der daraus resultierenden Weichgewebedeformation mittels der Finite-Elemente Methode (FEM) ermöglichen. Die Methoden der 3D Schnittplanung an computergrafischen Modellen werden analysiert und eine 3D Osteotomieplanung an polygonalen Schädelmodellen entwickelt, die es ermöglicht, intuitiv durch Definition von Schnittlinien am 3D Knochenmodell, eine den chirurgischen Anforderungen entsprechende Schnittplanung unter Berücksichtigung von Risikostrukturen durchzuführen. Separierte Knochensegmente lassen sich im Anschluss interaktiv umpositionieren und die resultierende Gesamtanordnung hinsichtlich einer funktionellen Rehabilitation bewerten. Aufgrund des in dieser Arbeit gewählten, physikalisch basierten Modellierungsansatzes kann unter Berücksichtigung des gesamten Weichgewebevolumens aus der Knochenverlagerung direkt die resultierende Gesichtsform berechnet werden. Dies wird anhand von 13 exemplarischen Fallstudien anschaulich demonstriert, wobei die Prognosequalität mittels postoperativer Fotografien und postoperativer CT-Daten überprüft und belegt wird. Die Arbeit wird mit einem Ausblick auf erweiterte Modellierungsansätze und einem Konzept für eine integrierte, klinisch einsetzbare Planungsumgebung abgeschlossen.
    Description: In cranio-maxillofacial surgery, physicians are often faced with skeletal malformations that require complex bone relocations. Especially in severe cases of congenital dysgnathia (misalignment of upper and lower jaw) or hemifacial microsomia (asymmetric bone and tissue development), where multiple bone segments are to be mobilized and relocated simultaneously and in relation to each other, careful preoperative planning is mandatory. At present in clinical routine not all possible strategies can be planned and assessed with regard to functional rehabilitation. Moreover, the aesthetic outcome, i.e. the postoperative facial appearance, can only be estimated by a surgeon's experience and hardly communicated to the patient. On this account, a preoperative planning of complex osteotomies with bone relocations on a computerized model of a patient's head, including a reliable three-dimensional prediction and visualization of the post-surgical facial appearance is a highly appreciated possibility cranio-maxillofacial surgeons are longing for. This work, being performed at Zuse Institute Berlin (ZIB), addresses such a computer based 3D~surgery planning. A processing pipeline has been established and a simulation environment has been developed on basis of the software Amira, enabling a surgeon to perform bone cuts and bone rearrangements in an intuitive manner on virtual patient models. In addition, a prediction of the patients' postoperative appearance according to the relocated bone can be simulated and visualized realistically. For a meaningful planning of surgical procedures, anatomically correct patient models providing all relevant details are reconstructed from tomographic data with high fidelity. These patient models reliably represent bony structures as well as the facial soft tissue. Unstructured volumetric grids of the soft tissue are generated for a fast and efficient numerical solution of partial differential equations, describing tissue deformation on the foundation of 3D elastomechanics. The planning of osteotomies (bone cuts) for the mobilization and relocation of bone segments is performed in accordance to the planning on basis of life size replicas of a patient's skull, i.e. stereolitographic models. Osteotomy lines can be drawn on top of the polygonal planning models using suitable input devices. After evaluation of the consequence of a planned cut with regard to vulnerable inner structures (nerves, teeth etc.) the model is separated accordingly. A relocation of bone segments can be performed unrestrictedly in 3D or restricted to a translation or rotation within arbitrarily chosen planes under consideration of cephalometric guidelines. Bone and tooth collisions can be evaluated for functional analysis or orthodontic treatment planning with possible integration of digitized dental plaster casts. As a result of the preoperative planning, a single transformation matrix, encoding translation and rotation, or a sequence of such matrices are provided for each bone segment. Both the osteotomy paths and the transformation parameters can finally be used for intra-operative navigation. In the course of the planning, the relocated positions of bone segments serve as an input for the simulation of the resulting soft tissue deformation. Since bone and surrounding soft tissue share common boundaries that are either fixed or translocated, the resulting configuration of the entire tissue volume can be computed from the given boundary displacements by numerical minimization of the internal strain energy on basis of a biomechanical model, using a finite-element approach. In collaboration with different surgeons and hospitals more than 25 treatments have been accompanied by preoperative planning so far ranging from mandibular and midfacial hypoplasia to complex hemifacial microsomia. 13 of these cases are presented within this work. Simulation results were validated on the basis of photographs as well as of postoperative CT data, showing a good correlation between simulation and postoperative outcome. Further aspects of improving the modeling approach are discussed. It has been demonstrated that 3D~osteotomy planning on virtual patient models can be performed intuitively, and that 3D~tissue deformation for cranio-maxillofacial osteotomy planning can be predicted numerically without using heuristic ratios. It can be stated that by using 3D~planning software, a surgeon gains a better spatial understanding of complex dysplasia, and the 3D~soft tissue prediction gives an additional criterion for the assessment of the planned strategy. It turned out that, especially in complex cases such as hemifacial microsomia or for decisions bet­ween mono- and bimaxillary advancements, a 3D~planning aid is extremely helpful. The conclusion is, that images and animations created within the planning phase provide a valuable planning criterion for maxillofacial surgeons as well as a demonstrative information for patients and their relatives, thus greatly enhancing patient information, as well as surgical education. All data that result from the planning are also important for documentation and quality assurance. 3D osteotomy planning, including soft tissue prediction, likely will become a new paradigm of plastic and reconstructive surgery planning in the future. An assortment of results can be found under: http://www.zib.de/visual/medical/projects
    Keywords: ddc:620
    Language: German
    Type: doctoralthesis , doc-type:doctoralThesis
    Format: application/pdf
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 279-286 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Convenient Synthesis of 4-Oxo-tetrahydropyrimidinesEnamino-nitriles as 6 or 11 yield 4-oxo-pyrimidines (2; 2a; 10; 12a-c) on treatment with cyclohexanone in basic media. Analogous compounds are obtained using acetone, butyraldehyde, benzaldehyde or substituted benzaldehydes.
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  • 10
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The “Normalizing Factor” for the Tomato Mutant chloronerva. XV. Peptide Analogues of the Phytosiderophore NicotianamineSome peptide analogues of the phytosiderophore nicotianamine, (2S, 3′S, 3″S)-N-[3-(3-amino-3-carboxypropylamino)-3-carboxypropyl]-azetidine-2-carboxylic acid, have been synthesized from protected amino acids by the EEDQ or the DCC method. They exhibited no biological effect with regard to the phenotypical normalization of the tomato mutant chloronerva.
    Type of Medium: Electronic Resource
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  • 11
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Aza-3-chloro-2-propeniminium salts 5, which are easily available by the addition of formamide chlorides 1 to nitriles 2 react smoothly with hydrazines 9 giving rise to 1,3-disubstituted 1,2,4,-triazoles 11. When the 2-aza-3-chloro-2-propeniminium salts 5 are hydrolysed first the resulting N-acyl-formamidinium salts 6 react with hydrazines 9 to 1,5 disubstituted 1,2,4-triazoles 13 via isolable N-acyl-formamidrazones 12.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 303-310 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Quantum Chemical Investigations of the Molecular and Electronic Structure of Simple Azomethine Imines and Related CompoundsThe molecular and electronic structure of simple azomethinimines are investigated by means of MINDO/3 and CNDO/2 calculations. The calculated molecular geometry is compared with X-ray results obtained for these compounds. Except for the NN-bond lengths MINDO/3 satisfactorily describes the molecular structure of azomethinimine and related π-electronic systems. The charges at the atoms along the conjugated chain are alternating as in polymethines. The terminal carbon atom carries a negative charge. This charge brings about an appreciable shielding of this carbon atom such as found in the 13C-n.m.r. spectrum. This result does not contradict a stabilization of azomethinimines in the crystal via = CH…O=C interactions.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 320-328 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of Oligodeoxyribonucleotides on a Polystyrene Grafted Polytetrafluorethylene Support via Phosphotriester Intermediates
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 342-348 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Quinazolincarboxylic Acids. I. Quinazolin-4-on(2,4-dion)-3-acetic Acids and Esters
    Additional Material: 6 Tab.
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 374-380 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effects of temperature, structure and sulphuric acid concentration on the selectivity of the oxidation of aliphatic ketones (R1COR2) (1a-g) by thallic sulphate have been investigated. With increasing temperature the quantity of internal α-hydroxyketone (3a-d) decreases and the quantity of 1-hydroxyketone (2a-d) increases in the oxidation of methyl alkyl ketones (R2〉CH3) (1a-d). The same concerns to the oxidation products of hexan-3-one (1e): 2-hydroxy-hexan-3-one (2e) and 4-hydroxy-hexan-3-one (3e), respectively. “The inverse selectivity temperature” (IST) for oxidation of linear methyl alkyl ketones (1a-c) and hexan-3-one (1e) has been found. With the use of the linear free-energy relationship it has been found that the selectivity of the reaction decreases with increasing the polar and steric effects of substituents R1, R2. With increasing the sulphuric acid concentration the selectivity of the oxidation of methyl alkyl ketones (1a, 1d) increases.
    Additional Material: 3 Ill.
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  • 16
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 401-406 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electrophilic Reactions on the Maleimide Double BondThe aminosubstituted maleimides 1 are deprotonated to the anions 2, which are reacted with various electrophiles. By this way with heterocumulenes, acid chlorides and vinylogous acid chlorides the new acylated maleimides 3-6, 9, 10 are isolated. This reaction presents a method of direct acylation on the maleimide double bond.
    Additional Material: 1 Tab.
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  • 17
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Light Induced Polymer and Polymerization Reactions. 14. Radical Photopolymerization by Potassium Trisoxalato Cobaltate Arylonium Salts Systems.The photopolymerization of acrylamide (AA) by trisoxalato cobaltate ([Co(ox)3]3⊖) is inefficient because the produced nucleophilic ·CO2⊖-radicals are oxidized or they terminate with polymer radicals. If onium compounds are added to this system the initiation efficiency is increased as follows : p-CH3OC6H4N2⊕〉Ph2I⊕〉PhCOCH2S(CH3)2⊕〉Ph3S⊕. By means of quantum yield measurements a mechanism was proposed including the electron transfer from ·CO2⊖ to onium compounds. The produced radicals also initiate the polymerization of AA. The exponent m of the polymerization rate (vp ≍ [AA]m) is decreased from 1.4 to 1.1 in the presence of Ph2I⊕, deciding the decrease of termination reaction between ·CO2⊖ and polymer radicals. In comparison with K3[Fx(ox)3] the corresponding cobalt complex possesses higher polymerization quantum yields for AA.
    Additional Material: 6 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 505-510 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hammett-like Correlations between 13C-NMR Chemical Shifts and Substituent Constants on Aniles of p-Nitrocinnamaldehyde
    Additional Material: 1 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 849-852 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyanoethylation of HydroquinazolinonesBy the reaction of acrylonitrile with octahydroquinazolinone-spirocyclohexane (1), cyanoethyl-octahydroquinazolinone-spirocyclohexane (2) is formed. Compound 2 and hydrogen-peroxide yield 5a-cyanoethyl-5-oxo-perhydro-oxaziridino[3,2-j]-quinazolin-2-spirocyclohexane (5). 2-Phenyl-octahydroquinazolinone (7) and acrylonitrile form 3,5a-biscyanoethyl-2-phenyl-octahydroquinazolinone-(4) (8). Compound 8 and hydrogenperoxide yield 3-phenyl-4,5a-biscyanoethyl-4-oxoperhydro-oxaziridino[3,2-j]-quinazoline (9). Compound 9 rearranges with ferrous sulphate to 3,4a-bis-cyanoethyl-4-oxo-8a-hydroxy-2-phenyl-octahydro-quinazoline (10).
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 876-892 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: About the Photochromic and Thermochromic Effect of Benzil PhenylhydrazonesBenzil phenylhydrazone 1 synthesized from benzil and phenylhydrazine possesses s-trans-E configuration detected by means of quantum chemical calculations and its spectral data. Upon irradiation a photochromic process proceeds with a λ-shift Δ λ ≈ 80 nm. The photoproduct has an s-cis-Z configuration. The quantum yields of the EZ-isomerization measured by spectroscopic methods depend on solvent (ΦEZ= 0,077 in CH3OH, ΦEZ= 0,22 in n-hexane), but are independent of the excitation wavelengths and O2. Benzil N-methylphenylhydrazone 2 is inactive under stationary irradiation. Both the Z/E-isomerization of 1 and 2 are be sensitized by benzil and m-methoxyacetophenone. On the basis of kinetic measurements the quantum yields of sensitized reactions of 1 are calculated (ΦEZsens = 0,43; ΦZEsens = 0,57). In protic solvents benzil phenylhydrazone 1 has thermochromic properties caused by E/Z-isomerizations. The measured activation parameters of these reactions are small. It is assumed that both the photoinduced and thermal isomerizations proceed via azo intermediates, as indicated by flash photolysis experiments.
    Additional Material: 5 Ill.
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  • 21
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 899-909 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photooxidation of Leuco Dyes. VIII. Time Resolved Investigations of the Mechanism of the Photooxidation of Leucocrystal VioletThe photooxidation of leucocrystal violet has been reexamined by means of conventional and laser flash photolysis as well as spin trap experiments. Three radical transients have been observed and assigned to the cation radical (λmax ≈ 490, 530 nm), the neutral radical with one—NCH3—CH2 moiety (λmax ≈ 480 nm) and the triphenyl methyl radical derivative (λmax ≈ 400 nm).
    Additional Material: 10 Ill.
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  • 22
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 23
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 360-366 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Preparation of β-Substituted trans-Ethylene Diphenylphosphines and Sulphides by P(0) and P(S)-activated OlefinationMethylene bis-diphenylphosphine monoxide (3c) in tuluene reacts regiospecifically and stereoselectively with aldehydes in the presence of potassium tert-butoxide to ß-substituted transethylene diphenylphosphines 6, which can be oxidized to the sulphides 2 by sulphur in acetone. These sulphides 2 are to be obtained also directly from methylene bis-diphenylphosphine oxide sulphide 3b and methylene bis-diphenylphosphine disulphide 3d, respectively, under the same olefination conditions. But the yields are smaller and the purification of the raw products is much more difficult, if 3d is used.
    Additional Material: 1 Ill.
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  • 24
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 599-604 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The present work deals with the synthesis of 6-aryl-2-ethoxycarbonyl pyridazin-3(2H)-ones (2) as useful synthetic intermediates because they allow formation of a new hydrazides (3), hydrazidoyl chlorides (4) and the highly reactive nitrile imine species (5). Dimerization and reaction of the latter species with benzonitrile, benzaldehyde and their p-methoxy and p-nitro derivatives provides a convenient method for the synthesis of substituted 1, 2, 4, 5-tetrazines (6), 1, 2, 4-triazoles (7) and 1, 3, 4-oxadiazoles (8), respectively, with pyridazin-3(2H)-one moiety.
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  • 25
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 737-746 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyanic Acid Esters. 35. On Formation and Consecutive Reactions of N-Cyanato Phthalimide. New Specifically Activated and Blocked Isatoic Acid DerivativesDepending on the reaction conditions N-hydroxy-phthalimide affords on treatment with cyanogen bromide via N-cyanato phthalimide 2 the iminocarbonate 3 and isatoic acid derivatives 7 and 16. Both the latter react with nucleophiles as isatoic acid derivatives activated on the carboxylic group and protected on the carbamic group or vice versa, furnishing N,N-bis alkoxycarbonyl anthranilic acid amides 9, N-alkoxycarbonyl anthranilic acid amides 12, o-alkoxycarbonyl phenyl ureas 17 and the benzotriazepin-2,5-dione 14. The structures of the new compounds are proved by 1H-n.m.r. and 13C-n.m.r. measurements as well as independent synthesis.
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  • 26
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Deactivation Behaviour of Arenes and Heteroarenes. XLI. Structural and Environmental Effects on the Intramolecular [π4s + π4s]- Photocycloaddition Reaction of α, ω-Bis-(9-acridiziniumyl) - alkanes.Fluorescence characteristics, including quantum yields and decay times, and quantum efficiencies for the reversible intramolecular [π4s + π4s]- photocycloaddition reaction for a series of α, ω-bis-(9-acridiziniumyl)-alkanes have been measured in several solvents and they have been compared with those of the model compounds acridizinium-ion. and 9-methyl-acridizinium-ion. These parameters of the bichromophores depend on the number of CH2-groups of chromophor linkage. The title compounds investigated were divided into groups of common behaviour, and differences are due to increasing bond angle strain and coulomb-repulsion in the photocyclomer state.
    Additional Material: 2 Ill.
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  • 27
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 779-790 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Catalytic Dimerization of Acrylic Acid Derivatives by Palladium Complexes. IV. The Dimerization of Methyl Methacrylate.Methyl methacrylate has been dimerized to a mixture of 2.5-di(methoxycarbonyl)-hex-1-ene(1) and (E)-2.5-di(methoxycarbonyl)-hex-2-ene (2) by catalytic systems containing dichlorobis (nitrile)-palladium (II) complexes and silver tetrafluoroborate, Codimerization experiments with methyl acrylate show a lower reactivity of methyl methacrylate. Oxidative addition of ß-chloro methyl methacrylate to tetrakis (triphenylphosphine) palladium (O) gave ß-polladio methyl methacrylates (8, 9) suitable for model investigations of the catalytic reaction. A proposal is given for a mechanism via pd(IV) intermediates.
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  • 28
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 811-816 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 7 Tab.
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  • 29
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 804-810 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mass Spectrometric Fragmentation of 4-Substituted 5-Hydroxynaphth[2,1-d]1,3-oxathiol-2-onesThe mass spectra of 5-hydroxynaphth[2,1-d]1,3-oxathiol-2-ones 1a-1x have been studied. They show characteristic fragmentations with participation of neighbouring groups. Investigations of isotopically labelled 4-alkyl and 4-acyl derivatives give evidence for the formation of cyclic ionic structures.
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  • 30
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 823-828 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Dependence of UV-Spectra of Substituted Naphthalenesulfonic Acids upon the pH-Value - A Contribution in Order to Elucidate the Structure of Acid Azo Dyes
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  • 31
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 910-916 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A detailed kinetic analysis is presented of the transient sultone (A2) formation which proceeds thermally from a photogenerated intermediate species after flash excitation of bromo thymol blue and bromo xylenol blue in the presence of quinoline, pyridine and 4-methyl pyridine in toluene solution. The sultone ring cleavage is a bimolecular reaction with the base resulting in a hydrogen-bridged molecular complex (A1) which equilibrates consecutively with the most stable rotamer of the ion pair (A3). The rate constants for the latter reaction are controlled essentially by conformational changes rather than by the proper proton transfer.
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  • 32
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 924-934 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Diels-Alder-Reactions. IX. On the Formation and the Thermolysis of Isomeric TricyclopentadienesThe formation of isomeric tricyclopentadienes by codimerisation of cyclopentadiene with endo- and exo-dicyclopentadiene between 100 and 140°C in the liquid phase, and the retrodiene reaction of the main isomeres of the tricyclopentadiene fraction by gas phase thermolysis were studied kinetically between 230 and 310°C. The rate constants and the parameters of activation were determined.
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  • 33
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 941-946 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 10β;-Chloro-estra-1,4-dienes as Intermediates of the Introduction of a 9(11)-Double Bond in Estra-1,3,5(10)-trienesThe synthesis of 9(11)-didehydro-estra-1,3,5(10)-trienes 5 starting from estra-1,3,5(10)-trienes 1 is described. 1 can be transformed into the ketals 2 and 3 by means of isocyanuric acid chloride and an alcohol such as methanol or ethylene glycol in the absence of moisture.The ketals 2 and 3 are sensitive against hydrolysis and react in the presence of water and traces of acid under formation of chlorodienone 4. Dehydrochlorination of 2, 3 and 4 with potassium-tert.-butylate in dimethylsulfoxide gives the 9(11)-didehydro compounds 5. The reaction mechanism of the electrophilic addition of positive chlorine and alcohol to the aromatic A-ring of 1 is discussed.
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  • 34
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 955-961 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pyrylium Compounds. XXV. Quantum Chemical Calculations Concerning the Valence Isomerization of 2-Amino-2H-pyran and -thiopyranThe equilibrium 2-amino-2H-pyran 6 ⇌ 5-amino-2,4-dien-1-one 7 was investigated using the semi-empirical MINDO/3 and MNDO methods. In accordance with experimental findings for the substituted derivatives 1/2a-d, the introduction of a methyl group into the position 3 of 6 or the exchange of oxygen by sulfur shifts the equilibrium towards the cyclic structures 8 and 10, respectively. Polar solvents, the influence of which was estimated applying the reaction field approach as well as the solvaton theory, and entropy effects are calculated to favour the ring-open valence isomer 7. These results also correspond to experimental results.
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  • 35
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photocatalytical Systems. LXIV. Theoretical Investigations of the Charge Transfer and of the Photochemical Reactivity of d6 Transition Metal Complexes with π Acceptor LigandsQuantum chemical investigations concerning the charge transfer interactions between a d6 complex fragment and heterocyclic nitrogen ligands are reported. The influence of inductive, mesomeric and steric effects on the π acceptor ability of the isolated ligand and on the electronic structure of the pentacyano-ferrate(II) mixed ligand compounds has been investigated and possibilities to sensitize spectrally the Fe(CN)5L3- system (L= pyridine-type ligand) with regard to their photochemical reactivity are discussed.
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  • 36
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Investigations of the Photo-Fading of Tautomeric Azo Dyes. VI. The Photochemical Oxidation by Singlet Oxygen of Phenylazoacetylacetones and PhenylazopyrazolonesThe dye-sensitized photo-oxidation by singlet oxygen of phenylazoacetylacetones (1) and Phenylazopyrazolones (2) has been investigated. The photo-fading of dyes is accelerated in the presence of Methylene Blue, a sensitizer of singlet oxygen, in airsatured methanolAn excellent relationship exists between the fading-rate of a series of dyes (1) and Hammett-σ-constants. An unexpected trend was found for photo-fading of a series of dyes (2). The Hammett plot consists of two parts, with a negative slope derived from electron-releasing substituents and a positive slope derived from electron-withdrawing substituents. The anomalous photo-fading is due to an attack of singlet oxygen on the more reactive anion of the phenylazopyrazolones in the case of electron-withdrawing substituents. In methanol containing acetic acid the dyes (2) exist only as the hydrazone tautomers. Under these conditions the fading-rate show a linear relationship with σ-constants.
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 994-998 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Tab.
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  • 38
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 1008-1010 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
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  • 39
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 1016-1020 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Prostaglandins and Prostaglandin Intermediates. XI. Synthesis of Optically Active Bicyclic Lactones - Convenient Intermediates for 8-Methyl Prostaglandins
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  • 40
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 1027-1033 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Quinazoline Carboxylic Acids. III. Quinazolin-4-on-3-benzoic Acids and Esters
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 1034-1036 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fluorescence Properties of Polymethine Dyes with Bridged Chains
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  • 42
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    Keywords: Chemistry ; Organic Chemistry
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  • 43
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984) 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 44
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 1-11 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complex Catalysis. XV. Cationic η3-Allyl-bis(triorganylphosphite)nickel(II) Complexes as Catalysts for the Stereoregular Butadiene PolymerisationSynthesis and catalytic properties of [C3H5NiL2]PF6 complexes 1a-f with L = tri-ethyl-, -isopropyl-, -phenyl-, -o-tolyl-, -thymyl- and o-biphenylylphosphite are described. It is shown how electronic and steric effects of the phosphite ligands in these complexes control their catalytic activity and selectivity in 1,4-polymerization of butadiene.
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  • 45
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 12-22 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyfunctionalized N-Tensides. VII. Substitution and Elimination in the Reaction of 1,2-Dihalogenoalkanes with Amines1, 2-Dichloroalkanes, 1, 2-dibromoalkanes and mixtures of 1-bromo-2-chloroalkanes and 1-chloro-2-bromoalkanes react with primary or secondary amines and give both elimination and substitution products, often in a nearly 1:1 proportion.The elimination products are the cis and trans-1-halo-1-alkenes, the 2-halo-1-alkenes, the 1,3-and 2, 4-dienes and the 1-alkenes. The main substitution products are the 1, 2-bis-aminoalkanes. Physical dates, 1H-n.m.r.-spectra, surface tension values and CMC-dates are given.
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  • 46
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 23-28 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetik der Dimerisierung von Aminen durch Wasserstoffperoxid in Gegenwart von Fe(II)SO4 als KatalysatorDie Kinetik der Dimerisierung von Diethyl, n-Butyl- und tert.-Butylamin durch Wasserstoffperoxid in Gegenwart von Fe(II)-Ionen wurde untersucht. Die Reaktion ist bezüglich Fe(II)-Ionen und der Amine 1. Ordnung und 0. Ordnung betreffs Wasserstoffperoxid. Produkte der Dimerisierungsreaktionen sowie einige ihrer kristallinen Derivate wurden erhalten und identifiziert. Die Aktivierungsenergien für Diethyl-, n-Butyl- und tert.-Butylamin betragen 153, 130 bzw. 105 KJ mol-1. Ein Reaktionsmechanismus wurde aufgrund der experimentellen Beobachtungen vorgeschlagen.
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 29-34 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Configurational Assignment of Steroids with Primary and Secondary Amino Groups by CD Measurements of the Copper Succinimidate complexesThe CD spectra of the copper succinimidate complexes of 9 different steroids with a primary and 3 steroids with a secondary amino group were investigated. A good correlation between the sign of the Cotton effects in visible range and the chirality of the immediate neighbourhood of the nitrogen atom was observed. The results obey the earlier established octant rule for this chromophor.
    Additional Material: 6 Ill.
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 35-40 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermitase - A Thermostable Serine Protease. I. Synthesis of Alanine Peptide Esters as Substrates of the EnzymeThe synthesis of N-acetylated and N-succinylated peptide esters of alanine is described. The peptides are built up from the Z-Abkürzung: Z = Benzyloxycarbonyl, Ac = Acetyl, Suc = Succinyl, OMe = Methylester, MA = Mischanhydridmethode, E = Ether, PE = Petrolether, Etac = Ethylacetat, AcOH = Essigsäure, Dibu = n-Dibutylether, DMSO = Dimethylsulfoxid, DMF = Dimethylformamid, TEA = Triethylamin, Ac2O = Essigsäureanhydrid protected peptides by liquid phase fragment condensation and by acylation of the deprotected peptide esters. The kinetic parameters K m and K cat of some compounds are presented.
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 41-47 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermitase - A Thermostable Serine Protease. II. Synthesis of Substrate Analogous Peptide Chloromethyl Ketones as Irreversibly Acting InhibitorsThe preparation of dipeptide to pentapeptide chloromethyl ketones of alanine wth variation of the amino acid in the P1 and P2 positionNomenklatur für die individuellen Aminosäurereste der Peptide nach I. Schechter u. A. C. Berger, Biochem. Biophys. Res. Commun. 27, 157 (1967). of the peptides is described. The synthesis is performed by fragment condensation of N-acylated amino acids or peptides with the unprotected chloromethyl ketone derivatives of amino acids and peptides, respectively. Some examples of enzyme inactivation by peptide chloromethyl ketones are discussed.
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 54-62 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C-N.M.R. Investigation of Interannular Conjugation in Substituted PyrazolesThe correlation of the 13C-chemical shifts with the Hammet values for substituted 3-anilino-1, 5-diphenylpyrazoles (1a-k) and substituted 3-methyl-1, 5-diphenylpyrazoles (2a-g) provides evidence for extensive interannular conjugation only between the N-benzene-and the pyrazole rings, whereas in the capto-dative disubstituted system 1 extensive conjugation through the whole molecule is possible. The chemical shifts correlate well with the HMO-calculated π-electron densities. From a comparison of the chemical shifts of unsubstituted 1 and diphenylamine it can be concluded that the 1,5 -diphenylpyrazol-3-yl group has the same electronic effect as the phenyl group.
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 48-53 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermitase - A Thermostable Serine Protease. III. Synthesis of N-Acylated Peptide Methyl Ketones as Inhibitors Reversibly Bound to the EnzymeMethyl ketone derivatives of dipeptides to pentapeptides are used as suitable tools in the investigation of the non-covalent binding for subsite mapping of the active site of the enzyme. The synthesis is mainly performed by fragment condensation of N-acylated peptides or amino acids with methyl ketone derivatives of amino acids. These are prepared from the Z-protectedAbkürzungen: Ac = Acetyl, Z = Benzyloxycarbonyl, Boc = t-Butyloxycarbonyl, Suc = Succinyl, Glp = Pyroglutamyl, OBz = Benzylester, pNA = p-Nitranilid, CH3 = Methylketon, CH2Cl = Chlormethylketon, MA = Mischanhydridmethode, TEA = Triethylamin, NEM = N-Ethylmorpholin, CKEE = Chlorkohlensäureethylester, CKBE = Chlorkohlensäurebutylester, MeOH = Methanol, EtOH = Ethanol, AcOH = Essigsäure, Ac2O = Acetanhydrid, Etac = Ethylacetat, THF = Tetrahydrofuran, E = Ether, PE = Petrolether, DMF = Dimethylformamid, DMSO = Dimethylsulfoxid, DMAP = 4-(Dimethylamino)-pyridin cloromethyl ketones by catalytic hydrogenation. For the coupling steps the Z-protection is preferred. The peptide methyl ketones used in kinetic studies were N-protected by the Z, acetyl, Boc or pyroglutamyl residue.
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 73-80 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the autoxidations of 1-phenylprop-1-yne, 1-phenylbut-1-yne, and 1-phenyl-3-methylbut-1-yne a considerable attack at the C≡C triple bond takes place. Both products of the oxidative cleavage of the C≡C bond and products formed through the corresponding oxirenes were detected. The oxirenes rearrange via the isomeric ketocarbenes to ketenes, which yield the corresponding carboxylic acids or their esters. A part of the intermediate ketenes is oxidized with decarboxylation to lower ketones. All products were identified and quantitatively determined after LiAlH4 reduction to the corresponding alcohols.
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  • 53
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 63-72 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Solvatochromism of 4′-Dialkylamino-α-Cyano-Stilbene-4-Diazonium-Salts4′-Dialkylamino-stilbene-4-diazonium-salts are deep coloured compounds and give strong solvatochromism. 4′-Diethylamino-α-cyano-stilbene-4-diazonium-tetrafluoroborate was investigated in 52 different solvents and 3 binary solvent mixtures. With increasing solvent basicity the longest wave lenght absorption maximum (\documentclass{article}\pagestyle{empty}\begin{document}$ \nu^{\hspace{-5pt}\sim}_{\rm max} $\end{document}) decrease. Complex formation by crown ethers causes a decrease of \documentclass{article}\pagestyle{empty}\begin{document}$ \nu^{\hspace{-5pt}\sim}_{\rm max}$\end{document}, too. In solvents with dielectricity constants higher than about 15 dissociation effects superpose solvatochromism. The summary of experimental dates support the approach of specific nucleophilic solvatation of diazonium ions.
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  • 54
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 81-86 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ionization and Dissociation of Triphenylmethyl Halides in MethylendichlorideThe Winstein scheme is valid for triphenylmethyl halides in methylendichloride. The equilibrium of ionization and dissociaton has been determined by investigation of the ratio between the sum of concentrations of ionic species and the covalent form. Tritylbromide in methylendichloride shows an exothermic ionization but endothermic dissociation. In the case of tritylchloride ionization and dissociation are nearly independent on the temperature.
    Additional Material: 4 Ill.
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  • 55
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 87-91 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Influence of Styren Addition on the Ionization-Dissociation Equilibrium of Trityl Halides in Methylene DichlorideThe ionization-dissociation equilibrium in solutions of trityl halides in methylene dichloride is effected by the addition of π-donors as a function of the temperature. The intensity of the trityl absorption of trityl fluoride and trityl chloride is decreased as it can be shown by u.v.-spectroscopy. The trityl absorption of trityl bromide solutions in methylene dichloride is very sensitive towards temperature changes. Measurements of the equilibrium constants for the ionization - dissociation-equilibrium, when styrene is added to the solution, indicate a specific solvation effect by the styrene molecules, however, a stabilization of ion pairs by specific solvation due to styrene molecules does not occur.
    Additional Material: 3 Ill.
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  • 56
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 101-110 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A New Synthesis of 6H-1,3-ThiazinesA new method for the synthesis of 1,3-thiazines is described. The addition of nucleophiles to γ-isothiocyanatoallylchlorides (1a-j) leads to functionalisation and subsequent cyclisation (nucleophilic cyclofunctionalisation). Reaction of secondary amines or alcohols under catalysis by tert. amines gives numerous 2-dialkylamino- (3a-w) or 2-alkoxy-6H-1,3-thiazines (4a-p).
    Additional Material: 4 Tab.
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  • 57
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photoinduced Electron Transfer-Reactions of Arenediazonium Ions Complexed with Crown EthersThe photolysis (full light of a medium pressure Hg-lamp) of p-methylbenzenediazonium-tetrafluoroborate in the presence of the crown ether 18-crown-6 (1) yields mainly the products of a heterolytic dediazoniation via arene cations as intermediates. The quantum yield ϕges of the photolysis from p-methoxybenzenediazonium-tetrafluoroborat in CH2Cl2 decreases in the presence of 18- crowns-6 (1) from 0.66 to 0.08. In contrast to 1, the photolysis of arenediazonium salts in the presence of dibenzo-18-crown-6 (3) yields mainly the products of a homolytic dediazoniation as a consequence of an electron transfer from 3 to the diazonium ion. ϕges of this reaction increases with decreasing wavelength of the exciting light from 0.09 (436 nm) to 0.32 (366 nm). this wavelength dependence is explained by formation of a correlated radical pair after excitation. In agreement with this situation a photo-CIDNP-effect is observed in the 15N-n.m.r.-spectra of isotopically labeled arenediazonium salts complexed by 3 and benzo-18-crown-6(2). No photo-CIDNP-effect is observed in the presence of 1. This different behaviour of the EDA-complexes formed by arenediazonium salts with the two different groups of crown ethers 1 and 2, 3 is discussed as a control of the electron transfer-reaction by the structure of the frontier orbitals.
    Additional Material: 3 Ill.
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  • 58
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 121-128 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dicyclopentadiene Oxidation. IV. Oxidation of 4,5- and 8,9-Dihydro-dicyclopentadieneA mixture of exo- and endo-4,5-dihydro-dicyclopentadiene 5 and also pure endo-8,9-dihydro-dicyclopentadiene 7 and pure exo-dicyclopentadiene 10 was oxidized in the absence and in the presence of catalysts. The compounds containing the norbornene structure mainly gave the corresponding exo-epoxides. No catalytic effects were observed in the formation of these nor-bornene epoxides. Compound 7 containing only the cyclopentene structure mainly yielded the corresponding hydroperoxide 9. In this case a catalytic effect of epoxidation catalysts was observed: in the presence of such catalysts the epoxide was increased.The results obtained prove the mechanism of dicyclopentadiene oxidation proposed by us.
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  • 59
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 129-138 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Acylation of Heterocycles with Carbonic Acid Derivatives. IV. Reaction of Benzoxazolin-2-thione with Aryl Cyanates. Kinetics and MechanismThe arylcyanate benzoxazoline-2-thione (1) reaction in the presence and absence of the tertiary amines yields 1-aryloxyiminocarbonylbenzoxazoline-2-thione (2) and 2-thiocyanatobenzoxazole (4). A mechanism is proposed based on the influences of the reactants concentration, the concentration and basicity of tertiary amines, the solvent-water concentration, the arylcyanate substituents electronic effects on the reaction rate and the apparent activation parameters. This mechanism consists in the nucleophilic attack of the benzoxazoline-2-thione S-atom on the cyanate, followed by rearrangement through a four-center transition state.
    Additional Material: 8 Tab.
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  • 60
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 145-147 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: INDO Calculation of 15N-13C Coupling Constants in Simple Cyanines and Merocyanines
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  • 61
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 139-144 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Quantum-Chemical Calculations on Allyl-Type Radicals: Cycloalkenyl- and Cycloalk-1-enylmethyl RadicalsThe ability of the MINDO/3-HE-method for predicting various molecular properties was tested for cycloalkenyl- (1 to 4), cycloalk-1-enylmethyl-(5 to 8), and for the resonance-stabilized cyclic radicals (9 to 12). Close by it was established that the calculated heats of formation are largely correct. The electronic distribution in the allylic part of 1 to 12 is evidently too levelled.Based on the defination of allyl resonance energy (ARE - SZWARC (1948)) a mean value for the ARE of 1 to 8 is derived to 55 ± 12 kJ · mol-1.
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  • 62
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 222-232 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Carbon-13 Nuclear Magnetic Resonance Spectra of PhenylfulgidesThe carbon-13 chemical shifts are determined in a series of phenylfulgides in order to investigate steric and electronic influences of substituents. By means of the shift differences between suitably substituted compounds results can be obtained as to the relative variation of the rotation angles of the phenyl rings as well as to te angle alterations between the exocyclic double bonds and the anhydride ring. Introducing 4-CH3O- and 4-NO2-groups at the phenyl rings the substituent induced alterations of the carbon-13 chemical shifts and the π-polarization effects related with it are discussed.
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  • 63
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 233-247 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electronic and Steric Substituent Influences on the U.V./VIS-Absorption Spectra of Phenylfulgide IsomersThe u.v./vis spectral data of a large number of phenylfulgides (E-, Z-, E-E-, E-Z-, Z-E-, Z-Z-isomers, 1.8a-dihydronaphthalenes) are presented. An increase of the number of phenyl rings as well as substitution of the phenyl rings cause correlatable bathochromic spectral shifts. Steric influences became obvious by introducing methyl groups, by coplanarization of phenyl groups and in the series of isomers. By means of PPP calculations shifts in position and/or intensity of absorption bands are ascribed to the substituent effects.The calculated band polarization of E(E-E)-isomers are in agreement with the results of polarization spectra in oriented liquid crystal mesophases. The polarization spectra allow the assignment of the longwave absorption band to the S2 ← S0 and S1 ← S0 electronic transitions for E-E-Isomers with a C2v-symmetry.
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  • 64
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 248-252 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Cyanochalcone reacted with thiourea and guanidine to yield the corresponding pyrimidine derivatives 2 and 4. On the other hand, urea reacted with the same reagent under the same experimental conditions to yield the known urea derivatives 3. A new synthesis of polyfunction pyridine via reaction of 1a with malononitrile in presence of aniline could be developed. Similar to the behaviour of 1a, Compounds 1b, c reacted with malononitrile in presence of aniline to yield compounds 8 and 9. In contrast to the behaviour of compounds 1a-c, 1d reacted with malononitrile to yield the malononitrile derivatives 10 or 11 based on the reaction conditions. Mechanisms to account for formation of the reaction products were suggested.
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  • 65
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 253-258 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Gibberellins. CIII. Synthesis of 8-Amino-gibbanesFor investigations of the structure-activity relationships of gibberellin phytohormones the synthesis of 8-amino-gibbanes is described. The reaction pathway involves condensation of gibberellin C (1a) and its methylester 1b with primary amines to the corresponding azomethins 1c-11 followed by stereoselective NaBH4-reduction to 8α-amino gibbanes 2a-2r.
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  • 66
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    Topics: Chemistry and Pharmacology
    Notes: Studies on U.V./Vis Absorption Spectra of Azo Dyes. XI. General Relationships between Structure and Colour of Protonated Azo DyesThe U.V.-VIS spectra of a wide range of azo dyes having structural variations in both diazo and coupling components in acidic solution are discussed.The azonium cation can be regarded as a donor-acceptor chromophore. Thus, structural variations which give a bathochromic shift in λmax, are explained. The negative halochromism is also discussed with reference to this model.
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  • 67
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 287-302 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pyrylium Compounds. XXI. Structure and Tautomerism of Pseudobases of Unsymmetrically Substituted 2,4,6-Triarylpyrylium SaltsHydrolytic ring opening of unsymmetrically substituted 2,4,6-triarylpyrylium salts 11 results in a mixture of two tautomeric pseudobases, the penten-1,5-diones 13 and 14. In crystalline state as a rule one of these tautomers markedly predominates, whereas in solution a rapid equilibrium establishment occurs which can be followed by 1H-n.m.r. and u.v. spectroscopy (equilibrium ratio nearly 1:1). The 1H-n.m.r. spectroscopic structural assignment of the two isomeric forms was supported by u.v. spectroscopic studies using 1:1 mixtures of the chromophoric partial systems ArCOCH=CHPh and ArCOMe or the pseudobases 10 of symmetrically substituted 2,4,6-triarylpyrylium salts 9 as reference systems. From the mass spectra of the pseudobases 10 and 13/14 follows that - if hydrolysis of 11 is performed in media containing H218O - mass spectrometric isotopic analysis of the resulting 18O-labelled pseudobases allows no information to be made about the regioselectivity of the ring opening. - Novel starting pyrylium salts of type 9 and 11 are characterized by u.v./vis data and by transformation into the corresponding pyridine derivatives.
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  • 68
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    Topics: Chemistry and Pharmacology
    Notes: 2, 2-Disubstituted Cyclopentane-1, 3-diones. IV. Synthesis of Prochiral Intermediates for the Synthesis of 8-Methyl-prostaglandin C2 by Alkylation of 2-Methyl-cyclopentane-1, 3-dione with 1-Bromo-alk-2-ynes.2-Methyl-cyclopentane-1, 3-dione (1) is preferentially C-alkylated by 1-bromo-alk-2-ynes in aqueous sodium hydroxide solution. By this method it is possible to prepare 2,2-disubstituted-1, 3-diones (3-8), which can be converted into prochiral intermediates for 8-methyl-PGC2, containing the complete carboxylic side chain.
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  • 69
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 457-466 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Properties of Liquid Crystalline Derivatives of RhodanineSubstituted benzylidene-rhodanines 3-8 were prepared both by condensation of 1 a-f with suitable aldehydes and by acylation of 2a-g with substituted benzoyl chlorides or cinnamoyl chlorid. The mesomorphic properties of the compounds are discussed in respect to molecular structure with the aid of i.r.-, Raman- and u.v./vis-spectra of 3d, 3k, 4, 5, 6g, 8a. We have investigated the dielectric and electrooptic behaviour of 31.
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 515-518 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 71
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 524-528 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two Modified Pulse Sequences for the 13C NMR Spectroscopic Characterization of CHn Building Groups. An Effective Method for the Determination of n and for the Estimation of 1J(13C—1H)
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  • 72
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    Topics: Chemistry and Pharmacology
    Notes: Cationic Photopolymerization of Isobutylglycidyl Ether with Benzoine Derivatives/Arylonium Salts- or Benzildimethyl Ketal/Arylonium Salts-Initiator SystemsRadicals produced by photolysis of benzoine derivatives and benzile dimethylketale decompose arene diazonium salts (ArN2⊕), diphenyliodonium salts (Ph2I⊕) and triphenylsulfonium salts (Ph3S⊕), respectively. The carbenium ions or protons formed in this way can be used for the cationic polymerization of isobutylglycidyl ether (IBGE). The efficiency of this polymerization depends on the quantum yields of the onium salts decomposition. A reactivity ArN2⊕ 〉 Ph2I⊕ 〉 Ph3S⊕ was found. In the case of ArN2⊕ the salt decomposition is caused by electron transfer between the photolytically produced substituted benzylic radicals and the diazonium ions. It is assumed that by the decomposition of Ph2I⊕ and Ph3S⊕ intermediates occur, which give rise to some reversible reactions. Therefore, the quantum yields of onium salt decomposition are less than those of initiator photolysis. The rate of cationic polymerization of IBGE is also influenced by the anion of onium compounds. A sequence PF6⊖ 〉SbF6⊖ 〉BF4⊖ was found.
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  • 73
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complications in the Initiation of Cationic Polymerizations by Lewis Acids - Model Calculations for Antimony(V)halogenidsQuantum-chemical CNDO/2-calculations including geometry-optimization show that complex anions (X5Sb-Z-SbY5)⊖ are formed as a result of interaction between Lewis acids SbX5 and anions SbY5Z⊖ (X, Y, Z = F, Cl, Br). This interaction is very strong in the case of X, Z = F and Y = Br. When the complex anions decompose the simple anions with the greatest number of fluorine ligands are formed.The interaction between the two different Lewis acids SbX5 and SbY5 yields a random distribution of the ligands of both acids.During formation of the ions SbX4⊕ and SbXY5⊖ the anion with the greatest number of fluorine ligands is formed.The probability of the conversion Sb(V)-Sb(III) is higher for SbCl5 than for SbCl6⊖.
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 572-578 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Valeric, caproic, and heptanoic acid and their methyl esters were oxidized at 140°C by molecular oxygen. The oxidation mixtures were reduced by LiAlH4 and the mono- and dihydroxy compounds formed were analyzed gaschromatographically. From the results obtained one can conclude that nonbranched aliphatic acids and their methyl esters are attacked by the chain-carrying peroxy radicals at the different C—H bonds with almost the same regioselectivity as normal paraffins Only the ß- and to a smaller extent the α-positions are desactivated by the neighbouring carboxylic group.
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 588-593 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Spin Trapping. I. Investigation of Radical Reactions of Some 3-Nitrono-6-oxocyclohexadienes by ESR-SpectroscopyThe title compounds (3, 4 and 5) add O- and C-centered radicals to the nitrono group to yield spin adducts containing a 4-oxo-cyclohexadienyl group in the α-position (6, 7 and 8). These new nitroxylradicals undergo α- and ß-scission. The nitroxyl radicals and the paramagnetic decomposition products were detected by esr-spectroscopy.Further, a more general way of radical-induced decomposition was discussed.
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 594-598 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of 2-Cyano-3-methoxy-maleinimide with Methylene Active Compounds and EnaminesThe vinylogous ester 1 gives with methylenactive compounds 2 carbamoylmaleinimides 3, which cyclize to pyridonimides 4. Reactions of 1 with enamines form cyanomaleinimides 6-8 and aminopyridines 11.
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 633-637 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Reaction Behaviour of N-(3-Chlorobenzo[b]thiophene-2-carbonyl)-imino-dithiocarbonic Derivatives3-Chlorobenzo[b]thiophene-2-carbonyl-chloride 1 was treated with potassium rhodanide to afford the appropriate acyl isothiocyanate 3, which adds nucleophilic agents as amines and thioles in good yields.Addition of methanethiole and subsequent alkylation of the dithiocarbamate 7 gives S, S-dimethylimino-dithiocarbonate 8. 3-Chlorobenzo[b]thiophene-2-carboxamide 2 reacts with carbon disulphide and phenyl isothiocyanate by chlorine substitution and cyclisation to benzo[b]thieno[2, 3-e]thiazines 9, 10 or 11. The structure of the final products were determined by analytical and spectroscopical dates.
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 679-682 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of Phosphorylated Ureas and Uretthanes with Phosphoric Acid Phenylester Diamide Structural Units
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 683-685 
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    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 686-688 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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  • 81
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 82
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 721-728 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of enamines 1 derivatives of cyclohexanon- or cycloheptanon-2-carboxylic acid anilides with malononitrile gave in the first step 2-phenylcarbamoyl-cycloalkylideno-malononitriles 3, which in turn were converted into 1-oxo-2-phenyl-3-amino-4-cyano-cycloalkenoisoquinolines 4. Enamines containing an adjacent diphenylamidino group 6 reacted with malononitrile giving 1-phenylimino-2-phenyl-3-amino-4-cyano-cycloalkenoisoquinolines 7. The alkaline hydrolysis of 7 yielded 1-phenylamino-3-oxo-4-cyano-cycloalkenoisoquinoline 8.
    Additional Material: 2 Tab.
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  • 83
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Palladium-Catalyzed Telomerization of Isoprene in Alcoholic Mediums and its Consecutive ReactionsThe telomerization of isoprene with methanol to give dimethyloctadienylmethylethers by palladium-containing homogenous catalysts was investigated. It was found that the primary products of the catalysis undergo different consecutive reactions catalysed by the same catalytic systems. These reactions, i.e. isomerization, ether cleavage, interchange reaction and oligomerization were investigated in greater detail. A reaction scheme is developed and discussed.
    Additional Material: 2 Ill.
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  • 84
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    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 747-756 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Deactivation Behaviour of Arenes and Heteroarenes. XL. The Mechanism of the Reversible Intramolecular [π4s + π4s]-Photocycloaddition Reaction of α,ω-Bis-(9-acridiziniumyl)-alkanes.On electronic excitation the bichromophores deactivate by fluorescence and radiationless photophysical processes from its local excited state. Simultaneously, intramolecular interaction occurs between the excited chromophor and that in the ground state (i.e. by reversible energy migration or intramolecular excimer formation). The excimer rapidly collapses to the cyclomer assuming a common pericyclic transition state for the reversible photocycloaddition. In the pericyclic state the reaction is split into cyclomer formation or backformation of bichromophores in the ground state, respectively. This mechanism of the reversible intramolecular [π4s + π4s]- photo-cycloaddition reaction is discussed on the basis of a potential correlation diagram.
    Additional Material: 7 Ill.
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  • 85
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 765-778 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Improved synthetic pathways to the cyclol system of ergot peptide alkaloids.As demonstrated in the case of N-tert. butyloxycarbonylhydroxyglycine, N-protected 2-hydroxy-2-amino acids can be directly condensed with dipeptide esters to afford tripeptide derivatives, which are activated C-terminally and transferred into the epimers (8) and (9) of the corresponding oxacyclols. These are separated in the usual manner into the aci and the naturally occuring configuration 2R:5S:10aS:10bS. Alternatively, the epimeric cyclols may be obtained by acylation of dipeptide lactams with 2-tert. butyloxycarbonylamino-2-benzyloxy-carboxylic acids, followed by hydrogenolytic debenzylation and cyclisation of the OH-deprotected acyl lactam.
    Additional Material: 2 Tab.
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  • 86
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    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 791-798 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple laboratory synthesis of gonadoliberin was elaborated basing on classical solution methods and using minimal protection of side-chain functions. In the final step a hexapeptide segment was condensed with the corresponding tetrapeptide and the obtained product was purified by a single step silica gel chromatography. The total efficiency of the whole synthesis was 15%.
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  • 87
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    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 799-803 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 6(α-Styryl)pyridazin-3(2H)-ones (1a-e) reacted with phenylmagnesium bromide and/or methylmagnesium iodide to give the 1,4-addition products, 4-phenyl and/or 4-methyl-6-(α-styryl)pyridazin-3(2H)-ones (3a-e). The structures assigned to the products are established by electronic and infrared spectroscopy and by synthesis of authentic samples in most cases.
    Additional Material: 1 Tab.
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  • 88
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    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 817-822 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
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  • 89
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    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 917-923 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Arylamino-thiophene-3-carboxylic Acid DerivativesThe title compounds 3 are synthesized by reaction of 2-amino-thiophene-3-carboxylic acid derivatives 1 with anilines. The nucleophilic 5-position in 3 allowed the synthesis of 5-aryliden-Δ3-thiolen-2-one-imines 5, 6 and the oxidative coupling to yield the azo compound 7. 1-Aryl-thieno-[2,3-d]pyrimid-4-ones 9, the thieno[2,3-b]chinolin-4-one 10 and the 4-chloro thieno[2,3-b]chinolines 10, 11 can be obtained from 3.
    Additional Material: 2 Tab.
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  • 90
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    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 935-940 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Spin Trapping of Radicals Formed during the Decomposition of Aromatic Diazonium Salts by UltrasoundThe decomposition of aromatic diazonium compounds ArN2⊕X⊖ (Ar = phenyl, 2,5-diethoxy-4-(N-morpholino)phenyl; X = BF4, PF6, B(C6H5)4, SCN, OCN,N3; 1a, 1c-f, 2b-f) by ultrasonic waves has been studied by e.s.r. The spin trapping technique has been shown to be a suitable method for the detection of free radical intermediates.
    Additional Material: 1 Tab.
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  • 91
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    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 947-954 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Palladium-Catalyzed Addition of Methanol to IsopreneThe soluble systems containing palladium(II)-compounds and tri-n-butylphosphine as a ligand catalyze the addition of methanol to isoprene to give methoxyisopentenes in goodyields. Activity and selectivity of the reaction are dependent on the ligand, the ratio ligand to palladium and in a surprising manner on the concentration of methanol.
    Additional Material: 6 Ill.
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  • 92
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    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 971-978 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of a Technical Fraction of Butene with TrichloroacetaldehydeIn pyrolysis plants for gasoline production a C4-fraction is formed containing isobutene, but-1-ene and but-2-ene as main products. The reactive separation of this fraction represents an industrial problem. One way to solve this problem is the reaction of trichloroacetaldehyde with these components to form addition products. The favoured reaction is the formation of 1,1,1-trichloro-4-methyl-pent-4-en-2-ol (1) and 1,1,1-trichloro-4-methyl-pent-3-en-2-ol (2) from iso-butene. The other isomers react very slowly. The influence of different reaction parameters was investigated to find a method for a reactive separation of the C4-fraction.
    Additional Material: 1 Ill.
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  • 93
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 999-1002 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Preparative Electrolytic Oxidation of n-Propyl Alcohol
    Additional Material: 1 Ill.
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  • 94
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 1025-1026 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chloro-Nitrosyl-Molybdenum-Complexes as Epoxidation Catalysts. III. About the Influence on the Liquid-Phase Oxidation of Olefinic Hydrocarbons
    Additional Material: 1 Tab.
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  • 95
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 96
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 97
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    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 381-384 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 9-Anthraldehyde (1), under the conditions of a benzoin condensation, yields 9-anthracenecarbonitrile (2). 9-Cyano-10-anthraldehyde (6) has been shown to be the likely intermediate in this reaction. Mesitaldehyde (7), under similar conditions, yields 2-hydroxy-2-mesitylethanoic amide (8).
    Additional Material: 1 Tab.
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  • 98
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    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 385-400 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electrochemical Reduction of 4-Substituted 7-Nitro-benzo-furazansThe electrochemical properties of 4-methoxy-, hydroxy-, alkylamino, and arylaminosubstituted 7-nitrobenzofurazans (1a-1h) are studied between pH 1,7 and 11,6 by use of buffer solutions containing different portions of various organic solvents. Reduction waves which are present in polarograms, are well reproducible and practicable for qualitative and quantitative analysis of amines. A mechanism of reduction is suggested by reason of polarographic and coulometric results. The half wave potentials are correlated with various substituent constants. A value of ϱ = + 0,32 follows from the determination of the reaction constant from the slope of the E 1/2 - σp - relation for the polarographic reduction of each nitro-function.
    Additional Material: 8 Ill.
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  • 99
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: β-Fur-2-yl-α-halogenacrylonitriles. I. Preparation of β-Fur-2-yl-ß-aminoacrylonitriles and β-Fur-2-yl-α-aminoacrylonitrilesβ-Fur-2-yl-α-halogenacrylonitriles 1 react with secondary amines to yield β-fur-2-yl-ß-aminonitriles 2 and β-fur-2-yl-α-aminoacrylonitriles 3. The 1 H-n.m.r. spectra of the E/Z isomers are discussed.
    Additional Material: 3 Tab.
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  • 100
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    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 326 (1984), S. 545-555 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: About Chlorination of N-Aryl-2,4-dimethyl-buta-1,3-dien-1,4-sultamesThe sultames of structure 1 are easily chlorinated by sulfurylchloride, chlorine or tertbutylhypochlorite. The structure of the mono-(2a-c,3a, d), di-(4a-d), tri- (5c, d) and pentachlorosultames (6a, b) is determined by 13C-n.m.r. spectroscopy. Contrary to the bromination the chlorination (by SO2Cl2) starts with the substitution of the sultamring (formation of mono- and di-chlorosultames) followed of the substitution of the (C-4)-CH3- group (formation of trichlorosultames). By 1,4-addition of an other molecule of chlorine to 5 the pentachlorosultames 6a, b are obtained. Already by recrystalisation of 6a, b in an alcohol the chlorine in 4-position is exchanged by the corresponding alkoxy group (CH3O, C2H5O, n-C3H7O) and the compounds 7-9 are formed.
    Additional Material: 5 Tab.
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