4.5 Article

Temperature-Controlled Divergent Synthesis of Tetrasubstituted Alkenes and Pyrrolo[1,2-a]indole Derivatives via Iridium Catalysis

期刊

ASIAN JOURNAL OF ORGANIC CHEMISTRY
卷 10, 期 12, 页码 3308-3320

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ajoc.202100476

关键词

Iridium; C-H activation; [3+2] annulation; Tetrasubstituted alkene; pyrrolo[1,2-a]indole

资金

  1. Zhejiang Provincial Natural Science Foundation of China [LQ19B020003, LY21B020003]
  2. Science and Technology Program of Sichuan Province [2018JY0345]
  3. National Natural Science Foundation of China [21602022]
  4. Chengdu Talents Program
  5. 1000 Talents Program of Sichuan Province
  6. Chenghua District Talents Program
  7. Jinhua Branch of Sichuan Industrial Institute of Antibiotics [1003, SIIAJH-202002, SIIAJH-202006]
  8. Jinhua Science and Technology Bureau [2021-3-150]
  9. Chengdu University [2081915037]
  10. Shanghai Pujiang Program [21PJ1415800]

向作者/读者索取更多资源

This novel method demonstrates excellent regio- and stereoselectivity, good substrate scope, and mild redox-neutral conditions, making it a versatile and efficient strategy for synthesizing tetrasubstituted alkenes and pyrrolo[1,2-a]indole derivatives.
We have achieved an Ir(III)-catalyzed temperature-controlled divergent synthesis of tetrasubstituted alkenes and pyrrolo[1,2-a]indole derivatives through C-H alkenylation/DG migration and [3+2] annulation, respectively. This method has various advantageous features: a) excellent regio- and stereoselectivity and good functional group tolerance, b) broad substrate scope and moderate to excellent yields, c) mild redox-neutral reaction conditions and operational simplicity.

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