Abstract
This review is about using lipases as catalysts in organic synthesis. It provides some specific examples of stereoselective biotransformations used in our group to prepare non racemic chiral building blocks and the utilization of these intermediates to synthesize different target molecules by organic transformations.
Keywords: lipases, enzymatic resolution, building blocks, natural products, enantioselective syntheses, absolute configurations
Mini-Reviews in Organic Chemistry
Title: Lipases-Promoted Enantioselective Syntheses of Monocyclic Natural Products
Volume: 2 Issue: 3
Author(s): Honore Monti and Gerard Audran
Affiliation:
Keywords: lipases, enzymatic resolution, building blocks, natural products, enantioselective syntheses, absolute configurations
Abstract: This review is about using lipases as catalysts in organic synthesis. It provides some specific examples of stereoselective biotransformations used in our group to prepare non racemic chiral building blocks and the utilization of these intermediates to synthesize different target molecules by organic transformations.
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Cite this article as:
Monti Honore and Audran Gerard, Lipases-Promoted Enantioselective Syntheses of Monocyclic Natural Products, Mini-Reviews in Organic Chemistry 2005; 2 (3) . https://dx.doi.org/10.2174/1570193054368855
DOI https://dx.doi.org/10.2174/1570193054368855 |
Print ISSN 1570-193X |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6298 |
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