4.5 Article

Ir-Catalyzed Enantioselective Hydrogenation of 2H-1,4-Benzoxazines with a Chiral 1,2,3,4-Tetrahydro-1-naphthylamine Derived Phosphine-aminophosphine Ligand

Journal

CHINESE JOURNAL OF CHEMISTRY
Volume 30, Issue 11, Pages 2664-2668

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cjoc.201200944

Keywords

asymmetric catalysis; hydrogenation; iridium; 2H-1; 4-benzoxazine; phosphine-aminophosphine ligand

Funding

  1. Dalian Institute of Chemical Physics (CAS)

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Unsymmetrical hybrid chiral phosphine-aminophosphine ligand derived from 1,2,3,4-tetrahydro-1-naphthylamine has been found to be highly efficient in the Ir-catalyzed asymmetric hydrogenation of various 3-aryl-2H-1,4-benzoxazines, providing good enantioselectivities (up to 95% ee) and high catalytic activity (S/C up to 5000).

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