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Rapid chromatographic technique for preparative separations with moderate resolution

W. Clark Still, +2 more
- 01 Jul 1978 - 
- Vol. 10, Iss: 2, pp 2923-2925
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Abstract
(11) Potassium ferricyanide has previously been used to convert w'c-1,2-dicarboxylate groups to double bonds. See, for example, L. F. Fieser and M. J. Haddadln, J. Am. Chem. Soc., 86, 2392 (1964). The oxidative dldecarboxylation of 1,2-dlcarboxyllc acids is, of course, a well-known process. See Inter alia (a) C. A. Grob, M. Ohta, and A. Weiss, Helv. Chim. Acta, 41, 1911 (1958); and (b) E. N. Cain, R. Vukov, and S. Masamune, J. Chem. Soc. D, 98 (1969).

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Peptidic phosphonylating agents as irreversible inhibitors of serine proteases and models of the tetrahedral intermediates.

TL;DR: A detailed kinetic analysis of the enzyme-inhibitor interactions was complicated by the susceptibility of the inhibitors to enzymatic degradation, and the configuration at phosphorus was found not to have a significant influence on the rate at which the inhibitors react with the peptidases.
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Mutagenicity of chlorine‐substituted furanones and their inactivation by reaction with nucleophiles

TL;DR: The reported high mutagenic potency of 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone against Salmonella typhimurium (TA100) was confirmed in the determined value of 6,300 net revertants/nmol as discussed by the authors.
Journal ArticleDOI

Effect of age and sex on the production of internal and external hydrocarbons and pheromones in the housefly, Musca domestica

TL;DR: The epicuticular and internal waxes of male and female houseflies were examined by capillary gas chromatography-mass spectrometry at closely timed intervals from emergence until day-6 of adulthood and Mathematical analysis indicated that the time shift between internal production and external accumulation in females is more than 24 h.
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Alkyl Substituent Effects on Pipecolyl Amide Isomer Equilibrium: Efficient Methodology for Synthesizing Enantiopure 6-Alkylpipecolic Acids and Conformational Analysis of Their N-Acetyl N'-Methylamides.

TL;DR: The results from the previous examination of N-acetyl-5-tert-butylproline N'-methylamides showed that the consequences of the bulky 6-alkyl substituent on the acetamide geometry and isomerization barrier were less pronounced in the pipecolate series relative to the respective proline amides.
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