An Enantioselective Bidentate Auxiliary Directed Palladium-Catalyzed Benzylic C−H Arylation of Amines Using a BINOL Phosphate Ligand
Volume: 55, Issue: 49, Pages: 15387 - 15391
Published: Nov 11, 2016
Abstract
A new enantioselective palladium(II)‐catalyzed benzylic C−H arylation reaction of amines is enabled by the bidentate picolinamide (PA) directing group. This reaction provides the first example of enantioselective benzylic γ‐C−H arylations of alkyl amines, and proceeds with up to 97 % ee . The 2,2′‐dihydroxy‐1,1′‐binaphthyl (BINOL) phosphoric acid ligand, Cs 2 CO 3 , and solvent‐free conditions are essential for high enantioselectivity....
Paper Details
Title
An Enantioselective Bidentate Auxiliary Directed Palladium-Catalyzed Benzylic C−H Arylation of Amines Using a BINOL Phosphate Ligand
Published Date
Nov 11, 2016
Volume
55
Issue
49
Pages
15387 - 15391
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