Issue 45, 2015

Organocatalytic direct difluoromethylation of aldehydes and ketones with TMSCF2H

Abstract

An organic Lewis base promoted direct difluoromethylation reaction of carbonyl compounds with Me3SiCF2H has been studied. The Schwesinger's superbase can efficiently activate the Si–CF2H bond and initiate the difluoromethylation of aldehydes and ketones under very mild conditions, producing difluoromethyl adducts in 42–99% yields.

Graphical abstract: Organocatalytic direct difluoromethylation of aldehydes and ketones with TMSCF2H

Supplementary files

Article information

Article type
Communication
Submitted
13 Mar 2015
Accepted
13 Apr 2015
First published
13 Apr 2015

RSC Adv., 2015,5, 35421-35424

Author version available

Organocatalytic direct difluoromethylation of aldehydes and ketones with TMSCF2H

G. Du, Y. Wang, C. Gu, B. Dai and L. He, RSC Adv., 2015, 5, 35421 DOI: 10.1039/C5RA04472C

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