Journal article
Metal-Free Reduction of Secondary and Tertiary N‑Phenyl Amides by Tris(pentafluorophenyl)boron-Catalyzed Hydrosilylation
Abstract
Tris(pentafluorophenyl)boron B(C6F5)3 is an effective catalyst for the hydrosilylative reduction of tertiary and N-phenyl secondary amides. It allows for the mild reduction of a variety of these amides in near quantitative yield, with minimal purification, at low temperatures, and with short reaction times. This reduction shows functional group tolerance for alkenes, nitro groups, and aryl halides, including aryl iodides.
Authors
Chadwick RC; Kardelis V; Lim P; Adronov A
Journal
The Journal of Organic Chemistry, Vol. 79, No. 16, pp. 7728–7733
Publisher
American Chemical Society (ACS)
Publication Date
August 15, 2014
DOI
10.1021/jo501299j
ISSN
0022-3263