4.8 Review

Organocatalysis in Inert C-H Bond Functionalization

Journal

CHEMICAL REVIEWS
Volume 117, Issue 13, Pages 9433-9520

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemrev.6b00657

Keywords

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Funding

  1. National Natural Science Foundation of China (NSFC) [21390400, 21572232, 21672217, 21521002]
  2. Ministry of Science and Technology (973 Program) [2011CB808600, 2012CB821600]
  3. Chinese Academy of Sciences [QYZDJ-SSW-SLH023]
  4. National Program for Support of Top-notch Young Professionals
  5. CAS Youth Innovation Promotion Association
  6. CAS one-hundred talented program (D)

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As two coexisting and fast-growing research fields in modern synthetic chemistry, the merging of organocatalysis and C-H bond functionalization is well foreseeable, and the joint force along this line has been demonstrated to be a powerful approach in making inert C-H bond functionafization more viable, predictable, and selective. In this review, we provide a comprehensive summary of organocatalysis in inert C-H bond functionalization over the past two decades. The review is arranged by types of inert C-H bonds including alkane C-H, arene C-H, and vinyl C-H as well as those activated benzylic allylic C-H, and C-H bonds alpha to the heteroatom such as nitrogen and oxygen. In each section, the discussion is classified by the explicit organocatalytic mode involved.

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