Abstract
Over the past decade, chiral Lewis base-catalysed cycloadditions has brought about numerous methods for the enantioselective synthesis of carbocycles and heterocycles. This short review covers some of the advances made in the area of absolute stereocontrol in this higher order cycloaddition.
Keywords: Cycloaddition, organocatalysis, asymmetric, Lewis base, phosphine catalysts, amine catalysts, organic synthesis, asymmetric cycloaddition, Diels-Alder transformations, carbocycles, heterocycles, cyclopropanes, alkaloids, bioactive molecules, stereochemistry
Current Organic Chemistry
Title: Catalytic Enantioselective Cycloaddition with Chiral Lewis Bases
Volume: 15 Issue: 24
Author(s): Claudia Lalli, Julien Brioche, Guillaume Bernadat and Geraldine Masson
Affiliation:
Keywords: Cycloaddition, organocatalysis, asymmetric, Lewis base, phosphine catalysts, amine catalysts, organic synthesis, asymmetric cycloaddition, Diels-Alder transformations, carbocycles, heterocycles, cyclopropanes, alkaloids, bioactive molecules, stereochemistry
Abstract: Over the past decade, chiral Lewis base-catalysed cycloadditions has brought about numerous methods for the enantioselective synthesis of carbocycles and heterocycles. This short review covers some of the advances made in the area of absolute stereocontrol in this higher order cycloaddition.
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Cite this article as:
Lalli Claudia, Brioche Julien, Bernadat Guillaume and Masson Geraldine, Catalytic Enantioselective Cycloaddition with Chiral Lewis Bases, Current Organic Chemistry 2011; 15 (24) . https://dx.doi.org/10.2174/138527211798109178
DOI https://dx.doi.org/10.2174/138527211798109178 |
Print ISSN 1385-2728 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5348 |
Call for Papers in Thematic Issues
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