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COAP/Pd-Catalyzed Linear Asymmetric Allylic Alkylation for Optically Active 3,3-Disubstituted Oxindole Derivatives with a Four-Carbon Amino Side Chain.

Wen-Kai LiuBai-Lin WangSheng-Suo ZhouJun-Hao ShenZheng WangXing-Wang Wang
Published in: Organic letters (2022)
An asymmetric linear selective allylic alkylation of vinylaziridines with 3-aryl oxindoles has been developed by using a chiral oxamide-phosphine (COAP-Bn-OMe- p )/palladium complex in methanol, which furnished a wide variety of 3,3-disubstituted oxindole derivatives in good yields with excellent regio- and enantioselectivities.
Keyphrases
  • structure activity relationship
  • solid state
  • room temperature
  • ionic liquid
  • reduced graphene oxide
  • capillary electrophoresis