rifamycin-s has been researched along with vinyl-acetate* in 1 studies
1 other study(ies) available for rifamycin-s and vinyl-acetate
Article | Year |
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Enzymatic desymmetrization of a meso polyol corresponding to the C(19)-C(27) segment of rifamycin S.
The stereoselective acylation of meso polyol 2 by vinyl acetate (solvent and acyl donor) in the presence of porcine pancreas lipase gave the corresponding monoester 5 in good yield (76%) and high enantiomeric purity (ee > 98%). The enzymatic reaction was also highly regioselective for a primary alcohol end group, and the two unprotected secondary alcohols were not involved. Compound 5 corresponds to the C(19)-C(27) fragment of rifamycin S. Topics: Acylation; Alcohols; Anti-Bacterial Agents; Binding Sites; Burkholderia cepacia; DNA-Directed RNA Polymerases; Fluorine; Gastrointestinal Agents; Magnetic Resonance Spectroscopy; Models, Molecular; Pancrelipase; Pseudomonas fluorescens; Rifamycins; Stereoisomerism; Vinyl Compounds | 2000 |