Journal
TETRAHEDRON LETTERS
Volume 59, Issue 18, Pages 1719-1722Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2018.03.058
Keywords
Silver-mediated; Radical; Aryltrifluoromethylthiolation; Activated alkenes; Oxindole
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Funding
- National Science Foundation of China [21572158]
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Herein, we describe the preparation of trifluoromethylthiol-substituted oxindoles by silver-mediated aryltrifluoromethylthiolation of activated alkenes, using S-trifluoromethyl 4-methylbenzenesulfonothioate as a F3CS radical source and showing that the reagent availability, mild conditions, and broad functional group compatibility of this transformation make it a viable alternative strategy of constructing C-sp3-SCF3 bonds. (C) 2018 Elsevier Ltd. All rights reserved.
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