4.3 Article

Some studies on nucleophilic trifluoromethylation using the shelf-stable trifluoromethylacetophenone-N, N-dimethyltrimethylsilylamine adduct

Journal

JOURNAL OF FLUORINE CHEMISTRY
Volume 126, Issue 4, Pages 491-498

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jfluchem.2004.11.010

Keywords

nucleophilic trifluoromethylation; trifluoromethyl carbinols; aldehydes; ketones; imines

Ask authors/readers for more resources

The simple thermal addition product of N,N-dimethyltrimethylsilylamine with 2,2,2-trifluoroacetophenone provides a shelf-stable reagent for nucleophilic trifluoromethylation of both the carbonyl and the imine group. (c) 2004 Elsevier B.V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available