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Department of Frontier Materials, Graduate School of Engineering, Nagoya Institute of Technology, Gokiso, Showa-ku, Nagoya 466-8555, Japan
E-mail: nozshiba@nitech.ac.jp
; Fax: (+) 81-52-735-5442
Org. Biomol. Chem., 2013,11, 1446-1450
DOI:
10.1039/C3OB27368G
Received
26 Nov 2012,
Accepted
14 Jan 2013
First published online
14 Jan 2013
A simple strategy avoiding the decomposition of a naked trifluoromethyl anion to difluorocarbene by a sterically very demanding organo-superbase without the help of a trifluoromethyl anion reservoir such as DMF is reported. The direct non-metallic trifluoromethylation of carbonyl compounds using fluoroform in the presence of t-Bu-P4 base afforded trifluoromethyl alcohols in high yields.
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Organic & Biomolecular Chemistry
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