4.8 Article

Rhodium-Catalyzed Reaction of Sulfoxonium Ylides and Anthranils toward Indoloindolones via a (4+1) Annulation

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ORGANIC LETTERS
卷 21, 期 17, 页码 6653-6657

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b02249

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资金

  1. National Natural Science Foundation of China [21572025, 21672028, 21602019]
  2. Innovation AMP
  3. Entrepreneurship Talents Introduction Plan of Jiangsu Province
  4. Natural Science Foundation of Jiangsu Province [BK20171193]
  5. Jiangsu Key Laboratory of Advanced Catalytic Materials Technology [BM2012110]
  6. Advanced Catalysis and Green Manufacturing Collaborative Innovation Center
  7. Young Natural Science Foundation of the Jiangsu Province [BK20150263]

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A rhodium-catalyzed annulation between aroyl sulfoxonium ylides and anthranils has been developed to synthesize 10H-indolo[1,2-a]indol-10-one derivatives. This reaction started with an unpredented (4 + 1) annulation toward N-(2-formylphenyl) indolones, proceeding with the sequential ortho-amination of the C-H bond in aroyl sulfoxonium ylides by anthranils and the insertion of N-H to carbene. Finally, the Aldol condensation constructed the second indole ring. This procedure features the formation of two C-N bonds and one C=C bond in one pot.

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