4.4 Article

Palladium-Catalyzed Aryl-Carbamoylation of Alkene-Tethered Carbamoyl Chlorides: Access to Diverse Aryl-Functionalized Oxindoles

期刊

CHEMISTRYSELECT
卷 6, 期 25, 页码 6464-6467

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.202101985

关键词

aryl-carbamoylation; carbamoyl chlorides; oxindoles; palladium-catalyzed; unactivated alkenes

资金

  1. National Natural Science Foundation of China [21901184, 21702091]
  2. Natural Science Foundation of Tianjin City [20JCQNJC00400]
  3. Doctoral Program Foundation of Tianjin Normal University [043135202XB1703]
  4. Program for Innovative Research Team in University of Tianjin [TD13-5074]

向作者/读者索取更多资源

By utilizing a palladium-catalyzed cascade strategy, an intermolecular aryl-carbamoylation of unactivated alkenes was developed under mild conditions, providing access to diverse aryl-functionalized oxindoles in moderate to good yields.
Utilizing a palladium-catalyzed cascade strategy, we have developed an intermolecular aryl-carbamoylation of unactivated alkenes under mild conditions, allowing for facile access to diverse aryl-functionalized oxindoles from alkene-tethered carbamoyl chlorides in moderate to good yields.

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