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Synthesis and in vitro evaluation of the antifungal activity of a series of thiomalic acid derivatives

✍ Scribed by Woodrow R. Byrum; John E. Wintter; Jack T. Bryan


Publisher
John Wiley and Sons
Year
1964
Tongue
English
Weight
285 KB
Volume
53
Category
Article
ISSN
0022-3549

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✦ Synopsis


Mono and diesters of thiomalic acid with various alcohols were prepared, and the S-n-butyl derivatives of the diesters were prepared. These compounds were analyzed, various physical constants were determined, and the fungicidal and fungisfatic activities were measured, usin undecylenic acid as the standard for comparlson against Tricbo ton men& mpfyter. Several of the compounds under the conditions o f z e tests e d i b i t e d fungicidal and/or fungistatic activity.

HIOMALIC ACID (mercaptosuccinic acid, 2-Tmercapto-l,4-butanedioic acid) possesses two structural features which are present in the structures of some commercially available antifungal compounds-namely, the -C-S-


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## Abstract The antifungal, naturally occurring acetylenic fatty acid 6‐nonadecynoic acid was synthesized in three steps (18 % overall yield), for the first time starting with commercially available 1‐tetradecyne. The synthesis developed herein will facilitate the further study of the antifungal pr