Synfacts 2007(7): 0731-0731  
DOI: 10.1055/s-2007-968662
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York

Iridium-Catalyzed Synthesis of Primary Allylic Amines from Allylic Alcohols

Contributor(s): Hisashi Yamamoto, Matthew B. Boxer
C. Defieber, M. A. Ariger, P. Moriel, E. M. Carreira*
ETH Zürich, Switzerland
Further Information

Publication History

Publication Date:
22 June 2007 (online)

Significance

The Carreira group has utilized sulfamic acid as an NH3 equivalent for the allylic substitution of allylic alcohols. Iridium was used at a loading of 1.5-3 mol% with phosphoramidite ligands. While much of the work focused on the use of a variety of substrates capable of performing in the allylic substitution reaction, one example of the catalytic asymmetric version was performed giving 70% ee, which was increased to 93% ee after trituration.