4.4 Article

Synthesis of propargylic and allylic trifluoromethyl selenoethers by copper-mediated trifluoromethylselenolation of propargylic chlorides and allylic bromides

Journal

TETRAHEDRON
Volume 70, Issue 46, Pages 8872-8878

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2014.09.091

Keywords

Trifluoromethylthiolation; Trifluoromethylselenolation; Copper; Propargylic trifluoromethyl selenoethers; Allylic trifluoromethyl selenoethers

Funding

  1. National Natural Science Foundation of China [21072030, 21372044]
  2. Research Fund for the Doctoral Program of Higher Education of China [20123514110003]
  3. SRF for ROCS, SEM, China [2012-1707]
  4. Science Foundation of the Fujian Province, China [2013J101040]
  5. Fuzhou University [022318, 022494]

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The copper-mediated trifluoromethylselenolation of propargylic chlorides and allylic bromides is described. This approach provides a wide range of propargylic and allylic trifluoromethyl selenoethers in moderate to good yields. These results open the way to synthesis strategies for various trifluoromethylselenolated compounds. (C) 2014 Elsevier Ltd. All rights reserved.

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