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Synfacts 2008(3): 0314-0314
DOI: 10.1055/s-2008-1042719
DOI: 10.1055/s-2008-1042719
Organo- and Biocatalysis
© Georg Thieme Verlag Stuttgart · New York
Metal-Free Reduction of Tertiary Amides
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.