Issue 24, 1998

Enantioselective palladium catalyzed allylic substitution with chiral thioether derivatives of ferrocenyl-oxazoline and the role of planar chirality in this reaction

Abstract

A series of chiral thioether dervatives of ferrocenyl-oxazolines, prepared with diastereoselectivities >95:5, have been shown to be highly efficient catalysts for a palladium catalyzed allylic substitution reaction, with enantioselectivity of 81–98% ee, and the role of planar chirality in these ligands was also discussed.

Article information

Article type
Paper

Chem. Commun., 1998, 2765-2766

Enantioselective palladium catalyzed allylic substitution with chiral thioether derivatives of ferrocenyl-oxazoline and the role of planar chirality in this reaction

S. You, Y. Zhou, X. Hou and L. Dai, Chem. Commun., 1998, 2765 DOI: 10.1039/A808267G

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