4.7 Article

Copper-catalyzed alkylarylation of activated alkenes using isocyanides as the alkyl source: an efficient radical access to 3,3-dialkylated oxindoles

期刊

CHEMICAL COMMUNICATIONS
卷 52, 期 38, 页码 6395-6398

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6cc02024k

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资金

  1. University of Leuven (KU Leuven)
  2. FWO Fund for Scientific Research Flanders (Belgium)
  3. China Scholarship Council (CSC)
  4. KU Leuven

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A novel and efficient protocol for the synthesis of 3,3-dialkylated oxindoles is described. The method involves a copper-catalyzed tandem radical addition/cyclization of N-arylacrylamides with the alkyl radicals generated from isocyanides. Two C-C bonds are formed in a single step.

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