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  • Chemistry  (11)
  • Porphyrins  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Analytica Chimica Acta 255 (1991), S. 413-416 
    ISSN: 0003-2670
    Schlagwort(e): Chemiluminescene ; Oxalate ; Porphyrins ; Urine
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 227-236 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Derivatives of Imidazolidines from Oxalic AmidinesTetraarylsubstituted oxalic amidines 1 react with acyl chlorides, phosgene, thiophosgene, chlorocarbonylsulfenylchloride, isocyaniddichlorides, and N-aroyl-1-chlorothio-formimidoylchlorides 7 to give the corresponding 5-membered heterocycles 3, 4, 5 and 8.Isocyanates 9 and isothiocyanates 10 react with oxalic amidines to yield imidazolidines 11, 12 and ureas 13, 14.Hydrolysis of 3-5, 8, 11, 12 leads to the corresponding oxo compounds 15, 16.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 322 (1980), S. 273-280 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The Reaction of N-Sulfinylamines with Isocyanides and Synthesis of 2,5-Diaryl-3,4-diarylimino-1,2,5-thiadiazolidin-S-oxidesN-Sulfinylamines 1 react with isocyanides 2 to give isocyanates 3, isothiocyanates 6, and especially 2,5-diaryl-3,4-diarylimino-1,2,5-thiadiazolidin-S-oxides 7.This new heterocyclic ring system 7 can also be synthesized in high yields by a cyclization reaction of tetraarylated oxalic amidines 9 with thionyl chloride.The acid catalyzed hydrolysis of the heterocyclic compounds 7 leads to oxalic anilides 8, the hydrolysis with alkali forms amidines 9. The amidine 9a reacts with N-sulfinyl-p-toluenesulfonamide 11 to give an open chained adduct 12.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 328 (1986), S. 805-811 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: MO-LCAO Calculations on Sulfur-containing π-Electron Systems. XLIX. Tetramethine Bridged Derivatives of the Oxalic Acid - Novel Coloured Pigments of Indigoid StructureWhereas thioamides react with the oxalylchloride to Δ2-thiazoline-4,5-diones 1, which are precursors of the versatile thioacylisocyanate 2 synthons, the analogous reaction between thioamides and oxalyl-bis(arylimidchlorides) completely fails. In the case of aliphatic thioamides the intermediate 2-methyl-Δ2-thiazoline-4,5-diimides 3 undergo oxydative dimerization. The poorly soluble products are tetramethine bridged heteroanalogous oxalates 4 or isomers. The u.v./vis spectra of the blue compounds are in favour with structure 4 rather than with structure 6. This conclusion has been drawn from the results of Pariser-Parr-Pople(PPP) type calculations. According to the calculated position of the colour band of the pigments and of different molecular subunits, and the correspondence of their electronic states involved in the excitation, the dye molecules can be thought as consisting of two symmetrically crossed polymethine chains. This structural feature is inherent to the H indigo chromophore.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 335 (1993), S. 95-97 
    ISSN: 0941-1216
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: On the Negative Solvatochromism of Cyclohexa-2,5-diene-1-thion Derivatives
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 334 (1992), S. 611-618 
    ISSN: 0941-1216
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 1,3-Acylrearrangements by Cyclisation of Thioureas with Imidochlorides of Oxalic Acid - An Approach to interesting Thiocarbonylic SystemsBy cycloacylation of various substituted thioureas with bis-imidochlorides of oxalic acid the new thiazolidines 3, 4 and isomeric imidazolidines 5, 6 are obtained. Especially when triethylamine is used as a base the main products are the deeply coloured 4-arylimino-5-thioxo-imidazolidines which can be regarded as s-cis-configurated 1,4-dihetero-1,3-dienes. Some thiazolidines can be rearranged by means of anhydrous organic acids to parabanic acid derivatives; whereas the 5-thioxo-imidazolidines result from an intramolecular 1,3-acyl rearrangement during the reaction.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 333 (1991), S. 555-559 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Deep Coloured Systems with Oxalic Acid Substructure-a Structural CorrectionBasing on a recent spectroscopic investigation the structure of earlier described deeply coloured systems derived from oxalic acid imidochlorides and thioacetamide has to be revised. Due to the poor solubility of these systems their spectroscopic characterization led to the misinterpretation as tetramethin-bridged thiazolines 1. By means of 1H-NOE-Difference-Spectroscopy of newly synthesized derivatives with lipophilic substituents a imidazolin-thion substructure 4 has been found. Such an arrangement of the heteroatoms clearly reflects a 1,3-rearrangement with participation of the oxalic acid system.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 333 (1991), S. 855-862 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Novel Steroidal Orthoesters by Intramolecular Cyclisation of Ethynylcarbinol Derivatives with Organic HypoioditesThe iodination of the 17β-acetoxy-17-ethynylsteroid 2 using iodine/copper(II)-acetate in combination with the nucleophiles acetic acid, water and methanol is reported. Examples for chemical modification of the products are described. A cyclisation occurs in the case of iodomethoxylation as a formal through-space 1.4-addition of the reagent forming a mixture of 4 isomer iodomethylen-1,3-dioxolanes. The configuration and ratio of the isomers as well as analytical data of this hitherto unknown dioxolane-system are given.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 332 (1990), S. 65-82 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: On the Reaction of Oxalic Amidines with Carbonic Acid Derived Heterocumulenes to Imidazolidine-DerivativesA useful synthetic route to nonsymmetric derivatives of imidazolidine (derivatives of parabanic acid) is demonstrated by the reaction of tetraarylated oxalic amidines 1 with different alkyl- and aryl substituted isothiocyanates 4, isoselenocyanates 31, and carbodiimides 30.Acylisothiocyanates 9 react differently leading to a mixture of three cycloacylation products 12, 13 and 14. Silylated heterocumulenes such as 25 and 26 react with 1 to give 28 and 29 transsilylation. Based on the 13C-n.m.r. spectroscopic investigation of the reaction between 1a and methyl isothiocyanate and phenyl isothiocyanate respectively a mechanism is proposed.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 332 (1990), S. 367-374 
    ISSN: 0021-8383
    Schlagwort(e): Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Investigations on Regioselectivity of Wittig-Horner and Reformatsky-Reactions on Selected 3,17-Dioxo SteroidsThe Reformatsky synthesis and the Wittig-Horner olefination of 3,17-dioxo steroids like androsta-1,4-diene-3,17-dione (ADD) 1 and androst-4-ene-3,17-dione (AD) 2 is described. There are differences in the regioselective introduction of identical substructures with these two methods resulting from different nucleophilicity and stereoelectronical relations of these two reagents. In Reformatsky synthesis the oxo group in 3-position predominantly reacts, whereas in the Wittig-Horner olefination (in the case of 1) the reaction occurs mainly in the 17-position.The structures of all new compounds has been confirmed by spectroscopical data.
    Materialart: Digitale Medien
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