Issue 8, 2005

C1 and C2-symmetric carbohydrate phosphorus ligands in asymmetric catalysis

Abstract

Carbohydrates are increasingly used as starting materials for the synthesis of enantiopure ligands. They contain a considerable number of stereocenters, and compounds with all possible configurational combinations are readily available. This tutorial review focuses on ligands obtained by the introduction of phosphorus functionalities (mainly phosphinite, phosphite or phosphine) into a carbohydrate framework. They are classified according to their structural features. In this review, ligands are organised as C1 ligands with a pyranoside or furanoside structure, and C2 ligands. Particular attention is paid to water soluble ligands prepared from carbohydrates. General methods for the preparation of the ligands are presented in order to show how the backbones can be obtained from simple carbohydrates. The catalytic results obtained in commonly studied processes are presented in tables in order to facilitate the comparison between the ligands. The advantages and limitations of the use of ligands based on carbohydrates are discussed.

Graphical abstract: C 1 and C2-symmetric carbohydrate phosphorus ligands in asymmetric catalysis

Article information

Article type
Tutorial Review
Submitted
09 Mar 2005
First published
09 May 2005

Chem. Soc. Rev., 2005,34, 702-713

C 1 and C2-symmetric carbohydrate phosphorus ligands in asymmetric catalysis

S. Castillón, C. Claver and Y. Díaz, Chem. Soc. Rev., 2005, 34, 702 DOI: 10.1039/B400361F

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