4.7 Article

Alkynyl trifluoromethyl selenide synthesis via oxidative trifluoromethylselenolation of terminal alkynes

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ORGANIC CHEMISTRY FRONTIERS
卷 2, 期 5, 页码 574-577

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5qo00045a

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资金

  1. National Natural Science Foundation of China (NSFC) [21372044]
  2. Research Fund for the Doctoral Program of Higher Education of China [20123514110003]
  3. Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry, P. R. China [2012-1707]
  4. Science Foundation of the Fujian Province, China [2013J01040]
  5. Fuzhou University [022318, 022494]

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The synthesis of alkynyl trifluoromethyl selenides by Cu-mediated oxidative trifluoromethylselenolation of terminal alkynes is reported. Treatment of [(bpy)Cu(SeCF3)](2) with various terminal alkynes in the presence of an oxidant, Dess-Martin periodinane, led to the formation of trifluoromethylselenolated acetylenes bearing sensitive moieties such as alkoxy, halogens, trifluoromethyl, and heterocyclic groups.

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