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Journal ArticleDOI

Rapid chromatographic technique for preparative separations with moderate resolution

W. Clark Still, +2 more
- 01 Jul 1978 - 
- Vol. 10, Iss: 2, pp 2923-2925
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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Chirale Synthesebausteine durch Kolbe‐Elektrolyse enantiomerenreiner β‐Hydroxy‐carbonsäurederivate. (R)‐ und (S)‐Methyl‐sowie (R)‐Trifluormethyl‐γ‐butyrolactone und ‐δ‐valerolactone

TL;DR: Chiral Building Blocks for Syntheses by Kolbe Electrolysis of Enantiomerically Pure β-Hydroxybutyric-Acid Derivatives as mentioned in this paper are used to prepare compounds with a 1.4 and 1.5-distance of the functional groups.
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Synthesis of potential inhibitors of hemagglutination by influenza virus: chemoenzymic preparation of N-5 analogs of N-acetylneuraminic acid.

TL;DR: N-Acylation of 2 produced several new N-acyl neuraminic acid analogs; these have been evaluated as inhibitors of adhesion of influenza virus to chicken erythrocytes in a hemagglutination inhibition assay (HAI).
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Antifungal phenanthrenes in yam tubers

TL;DR: An extract from the peel of yams showed anti-fungal activity towards both Cladosporium cladoporioides and a variety of ya.
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The synthesis of 7α-methyl-substituted estrogens labeled with fluorine-18: potential breast tumor imaging agents

TL;DR: In nearly every case, the 7 alpha-methyl substituent increases ER binding affinity and decreases binding to high affinity serum steroid binding proteins, alphafetoprotein, and sex steroid binding protein, but increases the lipophilicity and the predicted non-specific binding.
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