Lipases-Promoted Enantioselective Syntheses of Monocyclic Natural Products

Honore      Monti; Gerard      Audran

doi:10.2174/1570193054368855

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

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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

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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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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