4.8 Article

Rhodium(III)-Catalyzed Oxidative C-H/C-H Cross-Coupling of Heteroarenes and Masked Benzylamines

Journal

ORGANIC LETTERS
Volume 18, Issue 23, Pages 5998-6001

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b02773

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Funding

  1. National Natural Science Foundation of China [21572149]
  2. Young National Natural Science Foundation of China [21402133, 21403148]
  3. Major Basic Research Project of the Natural Science Foundation of Jiangsu Higher Education Institutions [15KJA150006]

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The first example of oxidative C-H/C-H cross coupling of oxalyl amide-protected benzylamines and various heteroarenes in the presence of a rhodium(III) catalyst has been developed. The route provides a means of synthesizing ortho-heteroarylated benzylamines. The methodology presents broad substrate scope, great functional group tolerance, and good to excellent yields in the synthesis of substituted benzylamines. The study also reveals that the thienoisoquinoline derivatives can be accessed through the intramolecular amination of thiophenyl-substituted benzylamines with palladium(II).

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