Issue 20, 1997

Asymmetric synthesis of keto-substituted P-chiral phosphines by means of an unusual exo/endo-stereochemically controlled Diels–Alder reaction

Abstract

An asymmetric Diels–Alder reaction between 1-phenyl-3,4-dimethylphosphole and ethyl vinyl ketone promoted by a chiral organopalladium complex gives the corresponding keto-substituted phosphine ligands in which the keto group can be stereospecifically located in the endo- or exo-positions of the phosphanorbornene skeleton.

Article information

Article type
Paper

Chem. Commun., 1997, 1987-1988

Asymmetric synthesis of keto-substituted P-chiral phosphines by means of an unusual exo/endo-stereochemically controlled Diels–Alder reaction

P. Leung, S. Loh, J. J. Vittal, A. J. P. White and D. J. Williams, Chem. Commun., 1997, 1987 DOI: 10.1039/A705830F

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