Jump to main content
Jump to site search

Issue 11, 2000
Previous Article Next Article

Trifluoromethylthiodediazoniation: a simple, efficient route to trifluoromethyl aryl sulfides

Author affiliations

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.

Back to tab navigation

Publication details

The article was received on 15 Feb 2000, accepted on 28 Apr 2000 and first published on 17 May 2000


Article type: Communication
DOI: 10.1039/B002560G
Citation: Chem. Commun., 2000,0, 987-988

  •   Request permissions

    Trifluoromethylthiodediazoniation: a simple, efficient route to trifluoromethyl aryl sulfides

    D. J. Adams, A. Goddard, J. H. Clark and D. J. Macquarrie, Chem. Commun., 2000, 0, 987
    DOI: 10.1039/B002560G

Search articles by author

Spotlight

Advertisements