Issue 16, 2002

Triphenylmethyldifluoramine: a stable reagent for the synthesis of gem-bis(difluoramines)

Abstract

The conversion of ketones into geminal bis(difluoramines) can be achieved under mild two-phase reaction conditions by employing triphenylmethyldifluoramine as an in situ source of difluoramine.

Graphical abstract: Triphenylmethyldifluoramine: a stable reagent for the synthesis of gem-bis(difluoramines)

Supplementary files

Article information

Article type
Communication
Submitted
16 Apr 2002
Accepted
13 Jun 2002
First published
10 Jul 2002

Chem. Commun., 2002, 1712-1713

Triphenylmethyldifluoramine: a stable reagent for the synthesis of gem-bis(difluoramines)

G. K. S. Prakash, M. Etzkorn, G. A. Olah, K. O. Christe, S. Schneider and A. Vij, Chem. Commun., 2002, 1712 DOI: 10.1039/B203811K

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