Issue 4, 2000

On the role of planar chirality: a tunable enantioselectivity in palladium-catalyzed allylic alkylation with planar chiral 1,1′-P,N-ferrocene ligands

Abstract

A series of planar chiral 1,1′-P,N-2′-substituted ferrocene ligands 9–12 and 16, prepared with diastereopurity >99∶1, have been used to examine the role of planar chirality, and significant effects on enantioselectivity as well as the control of absolute configuration in palladium-catalyzed allylic alkylation as a model reaction were observed.

Article information

Article type
Communication
Submitted
22 Nov 1999
Accepted
07 Jan 2000
First published
03 Feb 2000

Chem. Commun., 2000, 285-286

On the role of planar chirality: a tunable enantioselectivity in palladium-catalyzed allylic alkylation with planar chiral 1,1′-P,N-ferrocene ligands

W. Deng, X. Hou, L. Dai, Y. Yu and W. Xia, Chem. Commun., 2000, 285 DOI: 10.1039/A909211K

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