4.8 Article

Nickel-Catalyzed Dimerization and Alkylarylation of 1,3-Dienes with Alkyl Fluorides and Aryl Grignard Reagents

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 55, 期 18, 页码 5550-5554

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201601126

关键词

alkylation; dimerization; multicomponent reactions; nickel; regioselectivity

资金

  1. JSPS [25248025]
  2. MEXT [2204]
  3. Grants-in-Aid for Scientific Research [16H01150, 25248025] Funding Source: KAKEN

向作者/读者索取更多资源

In the presence of a nickel catalyst, 1,3-butadiene undergoes selective dimerization and alkylarylation with alkyl fluorides and aryl Grignard reagents to give 1,6-octadienes with alkyl and aryl groups at the 3- and 8-positions, respectively, by the consecutive formation of three carbon-carbon bonds. The formation of an anionic nickel complex plays an important role in forming C-C bonds with alkyl fluorides.

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