Lipases-Promoted Enantioselective Syntheses of Monocyclic Natural Products

Honore Monti; Gerard Audran

doi:10.2174/1570193054368855

ISSN: 1570-193X
E-ISSN: 1875-6298

Lipases-Promoted Enantioselective Syntheses of Monocyclic Natural Products
Authors: Honore Monti¹ and Gerard Audran²
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¹ Laboratoire de Reactivite Organique Selective, U.M.R. 6180 Universite Paul Cezanne-U3, F. S. T. St Jerome - 13397 Marseille Cedex 20, France. ² Laboratoire de Reactivite Organique Selective, U.M.R. 6180 Universite Paul Cezanne-U3, F. S. T. St Jerome - 13397 Marseille Cedex 20, France.
Source: Mini-Reviews in Organic Chemistry, Volume 2, Issue 3, Jul 2005, p. 265 - 281
DOI: https://doi.org/10.2174/1570193054368855
- Available online: 01 Jul 2005

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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2005-07-01

2025-05-08

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Article Type: Review Article

Keyword(s): absolute configurations; building blocks; enantioselective syntheses; enzymatic resolution; lipases; natural products

Lipases-Promoted Enantioselective Syntheses of Monocyclic Natural Products

Abstract

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