Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10596840 | Bioorganic & Medicinal Chemistry Letters | 2010 | 4 Pages |
Abstract
The first enantioselective biocatalytic synthesis of (S)-monastrol has been developed via an unexpected and unusual enzymatic pathway as suitable route. Whereas attempts for a direct hydrolysis of racemic monastrol were not successful, formation of racemic O-butanoyl monastrol and subsequent enantioselective hydrolysis furnished O-butanoyl (S)-monastrol with 97% ee. Cleavage of the O-butanoyl moiety then gave the desired (S)-monastrol with 96% ee.
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Authors
Maria Alfaro Blasco, Silvia Thumann, Jürgen Wittmann, Athanassios Giannis, Harald Gröger,