Issue 21, 2002

Facile axial chirality control by using a precursor with central chirality. Application to the preparation of new axially chiral diphosphine complexes for asymmetric catalysis

Abstract

A diastereoselective synthesis of a new chiral diphosphine with planar chirality is performed in 2 steps from (S)-p-tolylferrocenyl sulfoxide with 60% overall yield. The ligand gives enantioselectivities up to 98% ee in Pd(0)-catalyzed allylic substitution reactions.

Graphical abstract: Facile axial chirality control by using a precursor with central chirality. Application to the preparation of new axially chiral diphosphine complexes for asymmetric catalysis

Supplementary files

Article information

Article type
Communication
Submitted
29 Jul 2002
Accepted
06 Sep 2002
First published
01 Oct 2002

Chem. Commun., 2002, 2546-2547

Facile axial chirality control by using a precursor with central chirality. Application to the preparation of new axially chiral diphosphine complexes for asymmetric catalysis

M. Lotz, G. Kramer and P. Knochel, Chem. Commun., 2002, 2546 DOI: 10.1039/B207399D

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