4.7 Article

The benzoyl peroxide-promoted functionalization of simple alkanes with 2-aryl phenyl isonitrile

Journal

CHEMICAL COMMUNICATIONS
Volume 50, Issue 65, Pages 9179-9181

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4cc03304c

Keywords

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Funding

  1. National Natural Science Foundation of China [21272028, 21202013]
  2. Innovation & Entrepreneurship Talents Introduction Plan of Jiangsu Province
  3. Natural Science Foundation of Zhejiang Province [R4110294]
  4. State Key Laboratory of Coordination Chemistry of Nanjing University
  5. Jiangsu Key Laboratory of Advanced Catalytic Materials Technology
  6. Jiangsu Province Key Laboratory of Fine Petrochemical Engineering
  7. Priority Academic Program Development of Jiangsu Higher Education Institutions

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The benzoyl peroxide (BPO)-promoted phenanthridinylation of simple alkanes with isonitrile is developed via C(sp(3))-H and C(sp(2))-H bond cleavage. This procedure is featured by dual C-C bond formation proceeding with the addition of an alkyl radical to isonitrile followed by radical aromatic cyclization.

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