4.8 Article

Perfluoroalkylation of Unactivated Alkenes with Acid Anhydrides as the Perfluoroalkyl Source

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 55, 期 30, 页码 8740-8743

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201604127

关键词

alkenes; copper; homogeneous catalysis; perfluoroalkylation; peroxide

资金

  1. JSPS KAKENHI [15K17860]
  2. RIKEN
  3. Grants-in-Aid for Scientific Research [15K17860] Funding Source: KAKEN

向作者/读者索取更多资源

An efficient perfluoroalkylation of unactivated alkenes with perfluoro acid anhydrides was developed. Copper salts play a crucial role as a catalyst to achieve allylic perfluoroalkylation with the in situ generated bis(perfluoroacyl) peroxides. Furthermore, carboperfluoroalkylation of alkene bearing an aromatic ring at an appropriate position on the carbon side chain was found to proceed under metal-free conditions to afford carbocycles or heterocycles bearing a perfluoroalkyl group. This method, which makes use of readily available perfluoroalkyl sources, offers a convenient and powerful tool for introducing a perfluoroalkyl group onto an sp(3) carbon to construct synthetically useful skeletons.

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