Synthesis and in vitro evaluation of the antifungal activity of a series of thiomalic acid derivatives
β 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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β¦ 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-
π SIMILAR VOLUMES
## Abstract The antifungal, naturally occurring acetylenic fatty acid 6βnonadecynoic acid was synthesized in three steps (18 % overall yield), for the first time starting with commercially available 1βtetradecyne. The synthesis developed herein will facilitate the further study of the antifungal pr