Journal
TETRAHEDRON LETTERS
Volume 57, Issue 13, Pages 1397-1409Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2016.02.073
Keywords
Trifluoromethylthiolation; Nucleophilic; Trifluoromethyl thioethers; Reagent
Categories
Funding
- National Natural Science Foundation of China [21072030, 21372044]
- Research Fund for the Doctoral Program of Higher Education of China [20123514110003]
- SRF for ROCS, SEM, China [2012-1707]
- Science Foundation of the Fujian Province, China [2013J01040]
- Fuzhou University [022494]
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With regard to the high lipophilicity of the trifluoromethylthio group (CF3S-), there is a growing interest in the development of efficient methods for the incorporation of CF3S moiety onto organic molecules. In this review, recent advances in trifluoromethylthiolation using nucleophilic trifluoromethylthiolating reagents are discussed, highlighting some of the most intriguing examples of the synthesis of trifluoromethylthio-containing compounds using novel reagents. (C) 2016 Elsevier Ltd. All rights reserved.
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