Synfacts 2008(3): 0314-0314  
DOI: 10.1055/s-2008-1042719
Organo- and Biocatalysis
© Georg Thieme Verlag Stuttgart · New York

Metal-Free Reduction of Tertiary Amides

Contributor(s): Benjamin List, Subhas Chandra Pan
G. Barbe, A. B. Charette*
Université de Montréal, Canada
Further Information

Publication History

Publication Date:
21 February 2008 (online)

Significance

The authors report a chemoselective metal-free reduction of tertiary amides using Hantzsch ester 1 as the hydride source. Triflic anhydride was used as stoichiometric activating agent for this reaction. The authors have identified that functionalities such as esters, ketones, and epoxides are tolerated in their reaction and good to high yields (46-91%) are obtained for different tertiary amides.