Trifluoromethylthiodediazoniation: a simple, efficient route to trifluoromethyl aryl sulfides

Adams, D. J. , Goddard, A., Clark, J. H. and Macquarrie, D. J. (2000) Trifluoromethylthiodediazoniation: a simple, efficient route to trifluoromethyl aryl sulfides. Chemical Communications(11), pp. 987-988. (doi:10.1039/b002560g)

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Abstract

Copper(I) trifluoromethanethiolate reacts with a range of diazonium salts containing electron-withdrawing groups to give the corresponding trifluoromethyl aryl sulfides in high yield; it is also possible to carry out the diazotisation and trifluoromethylthiolation in one pot directly from the anilines.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Adams, Dave
Authors: Adams, D. J., Goddard, A., Clark, J. H., and Macquarrie, D. J.
College/School:College of Science and Engineering > School of Chemistry
Journal Name:Chemical Communications
Publisher:Royal Society of Chemistry
ISSN:1359-7345
ISSN (Online):1364-548X
Published Online:17 May 2000

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