4.8 Article

Nickel-Catalyzed Conversion of Enol Triflates into Alkenyl Halides

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 42, 页码 14901-14905

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201906815

关键词

alkenes; halides; kinetics; nickel; reaction mechanisms

资金

  1. National Science Foundation [DGE-1144469]
  2. NIH [R35GM118191-01]

向作者/读者索取更多资源

A Ni-catalyzed halogenation of enol triflates was developed and it enables the synthesis of a broad range of alkenyl iodides, bromides, and chlorides under mild reaction conditions. The reaction utilizes inexpensive, bench-stable Ni(OAc)(2).4 H2O as a precatalyst and proceeds at room temperature in the presence of sub-stoichiometric Zn and either 1,5-cyclooctadiene or 4-(N,N-dimethylamino)pyridine.

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