Resolution of a tetrahydrofuran ester by Candida rugosa lipase (CRL) and an examination of CRL's stereochemical preference in organic media

Volume: 7, Issue: 2, Pages: 497 - 510
Published: Feb 1, 1996
Abstract
Crude lipase from Candida rugosa (CRL) is able to resolve the C3-stereoisomers of the furo[2,3b]furan building block methyl 2-methoxytetrahydrofuran-3-carboxylate 6 by alcoholysis using n-butanol in octane. The reaction is not affected by the configuration at C2. The absolute configuration of the product 7 is 3S as determined by X-ray analysis of the crystalline derivative 14. The stereochemical outcome of the reaction is compared to the active...
Paper Details
Title
Resolution of a tetrahydrofuran ester by Candida rugosa lipase (CRL) and an examination of CRL's stereochemical preference in organic media
Published Date
Feb 1, 1996
Volume
7
Issue
2
Pages
497 - 510
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