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Enantioselectivity and diastereoselectivity in the hydrolysis of acylals and structurally related esters of secondary alcohols with Candida rugosa lipase

✍ Scribed by Yiannis S. Angelis; Ioulia Smonou

Publisher: Elsevier Science
Year: 1998
Tongue: French
Weight: 237 KB
Volume: 39
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(98)00256-1

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✦ Synopsis

Comparative studies of enantioselectivities and diastereoselectivities in the hydrolysis reactions of acylals and 50:50 threo-erythro mixtures of the esters of related secondary alcohols with Candida rugosa lipase gave significant information about the reactivity order in the enzymatic hydrolysis of acylals.

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