Issue 3, 2000

The bright future of stereoselective synthesis of co-ordination compounds

Abstract

Transfer of chirality during the build-up of molecules has been applied innumerable times in organic chemistry since the end of the 19th century, when it was introduced in the so-called asymmetric synthesis by E. Fischer. Although analogous reactions were introduced in co-ordination chemistry in its early development, diastereoselective reactions have not been applied in a very systematic way for co-ordination species. The highly versatile co-ordination geometry of metal centres makes the synthesis of a selected stereoisomer in general a formidable task. In the present article an account on new developments in the field is given, focussing on recently synthesized molecules, where natural chiral products are used to create a large number of chiral ligands which predetermine the chirality at metal centres.

Article information

Article type
Perspective
Submitted
02 Nov 1999
Accepted
22 Nov 1999
First published
27 Jan 2000

J. Chem. Soc., Dalton Trans., 2000, 219-231

The bright future of stereoselective synthesis of co-ordination compounds

A. von Zelewsky and O. Mamula, J. Chem. Soc., Dalton Trans., 2000, 219 DOI: 10.1039/A908730C

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