Issue 91, 2013

Catalytic enantioselective reductive desymmetrisation of achiral and meso compounds

Abstract

Herein an overview of reductive catalytic enantioselective desymmetrisation of achiral or meso compounds is provided. The most efficient reductive desymmetrisations described in the literature, which involve the reduction of C[double bond, length as m-dash]O, C[double bond, length as m-dash]N, C[double bond, length as m-dash]C and C–halogen bonds, or reductive ring-opening, are summarised. The structural diversity of the valuable highly enantioenriched intermediates prepared by reductive desymmetrisation is highlighted.

Graphical abstract: Catalytic enantioselective reductive desymmetrisation of achiral and meso compounds

Article information

Article type
Feature Article
Submitted
18 Jul 2013
Accepted
16 Sep 2013
First published
17 Sep 2013

Chem. Commun., 2013,49, 10666-10675

Catalytic enantioselective reductive desymmetrisation of achiral and meso compounds

H. Fernández-Pérez, P. Etayo, J. R. Lao, J. L. Núñez-Rico and A. Vidal-Ferran, Chem. Commun., 2013, 49, 10666 DOI: 10.1039/C3CC45466E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements