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Lipase-catalysed kinetic resolution of hydroxymethylchromanes

✍ Scribed by A. Czompa; T. Kovács; S. Antus


Book ID
102343315
Publisher
Journal of Heterocyclic Chemistry
Year
2000
Tongue
English
Weight
300 KB
Volume
37
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

An effective kinetic resolution of hydroxymethylchromanes racemic 2a and 3a has been achieved by means of enantioselective transesterification with vinyl acetate in organic solvents. The alcohols (‐)‐R2a and (‐)‐S3a were obtained with high optical purities (94 and 98% ee) in 70% and 38% yields, respectively. The influence of the enzyme source and the character of the solvent on the enantioselectivity were studied.


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