Journal
CHEMICAL COMMUNICATIONS
Volume 50, Issue 63, Pages 8768-8770Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4cc01610f
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An enantioselective hydrophosphination of beta,gamma-unsaturated alpha-ketoesters and amides has been developed using a chiral palladacycle catalyst. Adducts can be obtained in excellent yields and enantioselectivities, providing direct access to chiral tertiary phosphines which are synthetically useful intermediates in the preparation of bidentate ligands.
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