4.4 Review

Progress in Synthesis of Oxindoles by Radical Addition-Cyclization

Journal

CHINESE JOURNAL OF ORGANIC CHEMISTRY
Volume 34, Issue 10, Pages 1958-1965

Publisher

SCIENCE PRESS
DOI: 10.6023/cjoc201405006

Keywords

transition metal; metal-free; photoredox catalysis; oxindoles

Funding

  1. National Natural Science Foundation of China [21302042, 21172055]
  2. Program for Innovative Research Team from Zhengzhou City [131PCXTD605]

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In recent years, there are many reports about the synthesis of oxindoles by radical addition-cyclization. Most of these approaches are catalyzed by different transition metals, or under metal-free and photoredox catalysis conditions using N-arylacrylamides as main substrates. These methods have been a powerful strategy to obtain oxindoles in organic synthesis. At present, the studies on the synthesis of oxindoles by radical addition-cyclization are mainly focused on the types of radicals and the reaction mechanisms. This review will summarize the recent progress of the synthesis of oxindoles by radical addition-cyclization according to the different catalyst systems.

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