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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 299-305 
    ISSN: 0887-624X
    Keywords: polygluconamides ; stereoregular polyamides ; stereoregular nylons ; chiral polyamides ; chiral nylons ; aminoaldonic acids ; sugar polyamides ; carbohydrate monomers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two stereoregular polygluconamides, one (3) of polypeptide-type and the other (16) being a polycaproamide containing four stereocenters in the main chain of the repeating unit, have been prepared from D-glucosamine and D-glucose, respectively. The new polyamides were characterized by elemental analysis, and IR, 1H- and 13C-NMR spectroscopies. The molecular weights for 3 and 16 were estimated as 25,000 and 67,000, respectively, on the basis of viscosimetric measurements. Both polyamides display high optical activity; they are highly hydrophilic and readily soluble in water as well as in a variety of organic solvents including chloroform. Polyamide 16 is highly crystalline and yields resistant films with spherulitic texture. © 1995 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0899-0042
    Keywords: Circular dichroism ; helicity rule ; X-ray structure determination ; ultraviolet spectra ; n - π* and π - π* bands ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chiroptical properties of a series of 3 and/or 4-heterosubstituted 2(5H)-furanones were investigated with respect to correlation with absolute configuration. The n - π* and π - π* Cotton effects have been assigned on the basis of comparison with the UV spectra in solvents of varying polarity. It is demonstrated that the n - π* transition in 4-amino substituted 2(5H)-furanones appears at shorter wavelength with respect to the π - π* transition. With the exception of 4-pyrrolidino and 4-benzylamino substituted 2(5H)-furanones, other heterosubstituted 2(5H)-furanones follow the butenolide configurational rule (Gawronski et al. J. Org. Chem. 61:1513-1515, 1996). Absolute configuration of 2(5H)-furanone derivatives can also be assigned according to the sign of the Cotton effect (of unknown origin) at 200-230 nm. The structure of four representative sulfur and nitrogen substituted 2(5H)-furanones has been analyzed by X-ray diffraction. The results indicate planarity of the furanone ring and extended conjugation in 4-amino substituted 2(5H)-furanones. Chirality 9:537-544, 1997. © 1997 Wiley-Liss, Inc.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 10 (1995), S. 85-89 
    ISSN: 0884-3996
    Keywords: Human neutrophils ; ticlopidine ; oxygen-free radicals ; chemiluminescence ; luminol ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Neutrophils contribute to the pathophysiology of various ischaemic states. Since many agents thought to be antiplatelet have also been shown to affect neutrophil function, it was of interest to examine the effect of ticlopidine (250 mg, p.o., b.i.d. for three doses), an antiplatelet agent, on fMLP (formyl-methionyl-leucyl-phenylalanine) stimulated neutrophil aggregation and luminol-dependent chemiluminescence in whole blood. Neutrophil aggregation did not significantly change from baseline values during ticlopidine administration. However, luminol-dependent chemiluminescence, an index of respiratory burst metabolism, was noted to be markedly increased during ticlopidine administration. Two hours following the final dose of ticlopidine, the chemiluminescent response (mean ± SEM, n = 5) was significantly increased from 6.27 ± 1.88 to 12.66 ± 2.19 units (p 〈 0.05). A return to baseline (6.68 ± 2.24 units) five days following the administration of ticlopidine was noted. It is concluded from this study that the acute oral administration of ticlopidine may affect neutrophil function as demonstrated by the significant increase in stimulated luminol-dependent chemiluminescence.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie Ingenieur Technik - CIT 67 (1995), S. 1092-1093 
    ISSN: 0009-286X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 13 (1980), S. 396-402 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rotational barriers and 15N chemical shifts have been measured in a number of ureas and thioureas. As anticipated on the basis of the 15N shifts, several previously unobserved rotational barriers could be detected by using lanthanide reagents or a high field spectrometer. Nearly constant effects on both the rotational activation energy and the 15N shift are produced on going from ureas to the corresponding thioureas, and correlations are found between the ΔG
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 3 (1971), S. 661-677 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Coupling constants of 35 substituted pyridines are discussed and related to the electronic properties of the substituents and to the mechanism of coupling. A calculation of J is performed using Pople and Santry's theory and mutual polarizabilities obtained by CNDO/2 or Hoffmann methods. The influence of bicentric integrals on the theoretical values of J is examined.
    Notes: Les constantes de couplages relatives à un ensemble de 35 pyridines substituées sont discutées en relation avec les propriétés électroniques des substituants et le mécanisme du couplage. Un calcul de J est réalisé, sur la base de la théorie de Pople, à l′aide des valeurs de polarisabilités mutuelles obtenues par la méthode CNDO/2 et la méthode d'Hoffmann. L'influence d′une inclusion des intégrales bicentriques est examinée.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: A theoretical analysis of the proton chemical shifts of alkoxy-1,3-diene stereoisomers is proposed. The diamagnetic contribution is calculated from π and σ theoretical indices obtained by the CNDO/2 method. This effect depends on the stereochemistry of the molecule and the charges and chemical shifts alternate in the same way. The diamagnetic part is often small compared to the experimental value, however, and the paramagnetic contribution Δδp is important. Δδp is difficult to explain with the usual models of anisotropic and electric contributions, but the results give useful information on the conformations of the molecules.
    Notes: Une analyse théorique des déplacements chimiques protoniques de stéréoisoméres alcoxydiéniques est proposée. La contribution diamagnétique est évaluée à partir des indices théoriques π et σ obtenus par un calcul de type CNDO/2; ce terme qui dépend de la stéréochimie ne suffit pas à expliquer les écarts expérimentaux, bien que l'alternance des charges refléte celle des déplacements chimiques; la contribution paramagnétique est importante mais reste mal expliquée dans le cadre des méthodes approchées de calcul des effects d'anisotropie et de champélectrique. Cependant l'analyse des résultats apporte des informations sur la nature des équilibres conformationnels au niveau de la liaison=C—O—.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 6 (1974), S. 648-653 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Proton and carbon magnetic resonance spectra of mono-and disubstituted selenophenes are investigated. The proton chemical shifts are discussed in terms of magnetic anisotropy and electric field effects of the substituents, with a view to studying the conformational equilibrium of the carbonyl group. π Electronic charges, computed by the PPP method, are correlated with the proton and carbon chemical shifts. The coupling constants between 13C and 1H (1, 2 or 3 bonds) and 13C—77Se are shown to be good structural parameters and a set of substituent additivity constants is calculated.
    Notes: Une série de sélénophènes mono- et bisubstitués est étudiée en résonance de 1H et 13C. Les déplacements chimiques protoniques sont analysés en termes d'effets d'anisotropie et de champ électrique des substituants et utilisés à une discussion des équilibres conformationnels. Les relations entre δ1H et δ13C et les charges π calculées par la méthode PPP sont examinées. Les couplages 1J(13C—H), nJ(13C ∼ H) et 1J(13C—77Se) se révèlent de bonnes caractéristiques structurales et des relations d'additivité sont dégagées pour δ13C.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 17 (1981), S. 182-185 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The selective population transfer method has been applied to the study of a secondary amide and of the corresponding iminium salt. Important signal-to-noise enhancements were accessible in both fully coupled and proton decoupled 15N and 13C spectra. Moreover, the resolving power of the method was exploited for the accurate determination of long range 15N1H coupling constants. Experiments in which the selective inversion of transitions pertaining to the 15N satellite spectrum of multiplets which themselves constitute the 13C satellite spectrum of the main proton resonances could be carried out. The influence of a change from the amide to the iminium structure on the magnitudes and the signs of various 15N1H and 15N13C coupling constants is discussed.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 121-129 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: In Z—CH—CH=CH—Y compounds (Z or Y being an alkyl group) the ethylenic part of the spectra is often very complex and the 3J(H—C=C—H) coupling constant which is a good tool for determining the configuration, is not easily determined. We have studied such allylic derivatives and many configurations have been assigned through stereospecific synthesis. Except a very few cases, δ CH(Z) of the cis isomer is larger than δ CHZ of the trans isomer. In alcohols RCH=CH—CHOHR′ the stereoisomers behave differently in solutions with europium, praseodymium, holmium and dysprosium complexes. The spectra of the trans isomers remain strongly coupled but 3J(H—C=C—H) becomes easy to measure in the cis compounds.
    Notes: Dans les composés de structure Z CH—CH=CH—Y la complexité du spectre rend souvent difficile l'obtention du couplage J(H—C=C—H) et donc l'identification de la configuration. L'étude de nombreux dérivés de ce type préparés par des méthodes stéréospécifiques montre qu'à de rares exceptions près, le déplacement chimique δ CH(Z) de l'isomère cis est supérieur à δCH(Z) de l'isomére trans. Dans le cas des alcools R CH—CH CHOH R′ les isoméres configurationnels ont des comportements différents en présence de complexes d'europium ou de praseodyme, holmium et dysprosium. Si le spectre des isoméres trans reste fortement couplé en présence de complexe l'obtention de 3J(H—C=C—H) devient aisée dans les composés cis.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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