Issue 17, 2009

A perfect double role of CF3 groups in activating substrates and stabilizing adducts: the chiral Brønsted acid-catalyzed direct arylation of trifluoromethylketones

Abstract

A direct and efficient Brønsted acid-promoted arylation of tri- and difluoromethyl ketones, as well perfluoroalkyl ketones, has been developed; good to excellent enantioselectivities (up to 99% ee) were achieved.

Graphical abstract: A perfect double role of CF3 groups in activating substrates and stabilizing adducts: the chiral Brønsted acid-catalyzed direct arylation of trifluoromethylketones

Supplementary files

Article information

Article type
Communication
Submitted
09 Jan 2009
Accepted
16 Feb 2009
First published
09 Mar 2009

Chem. Commun., 2009, 2356-2358

A perfect double role of CF3 groups in activating substrates and stabilizing adducts: the chiral Brønsted acid-catalyzed direct arylation of trifluoromethylketones

J. Nie, G. Zhang, L. Wang, A. Fu, Y. Zheng and J. Ma, Chem. Commun., 2009, 2356 DOI: 10.1039/B900474B

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