4.7 Article

Enantioselective Rhodium-Catalyzed Addition of Arylboronic Acids to Trifluoromethyl Ketones

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 355, Issue 7, Pages 1297-1302

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201201125

Keywords

arylboronic acids; chiral phosphorus ligands; nucleophilic addition; rhodium; trifluoromethyl ketones

Funding

  1. State Key Laboratory of Bioorganic and Natural Products Chemistry

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A new C2-symmetrical, chiral bisphosphorus ligand proved to be efficient for the rhodium-catalyzed nucleophilic addition of arylboronic acids to trifluoromethyl ketones, providing a series of chiral trifluoromethyl-substituted tertiary alcohols in high yields (up to 93%) and excellent enantioselectivities (>99%).

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