4.4 Article

Amide-directed arylation of sp3 C-H bonds using Pd(II) and Pd(0) catalysts

期刊

TETRAHEDRON
卷 66, 期 26, 页码 4811-4815

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2010.03.111

关键词

Amide; Palladium; Arylation; sp(3) C-H activation

资金

  1. Scripps Research Institute
  2. National Institutes of Health (NIGMS) [1 R01 GM084019-02]
  3. Amgen
  4. Eli Lilly
  5. A.P. Sloan Foundation
  6. Bristol Myers Squibb

向作者/读者索取更多资源

Protocols to effect beta-arylation of sp(3) C-H bonds via Pd(II)/(IV) and Pd(0)/(II) catalytic cycles have been achieved using a newly developed monodentate CONHC6F5 directing group. These reactions provide an unprecedented means to functionalize sp(3) C-H bonds in aliphatic carboxylic acid-derived substrates. (C) 2010 Elsevier Ltd. All rights reserved.

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