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Highly diastereo- and enantioselective synthesis of multisubstituted allylic amino acid derivatives by allylic alkylation of a chiral glycine-based nickel complex and vinylethylene carbonates.

Chao YuYuyan YuLongwu SunXinzhi LiZhigang LiuMiao-Lin KeXiangtao Chen
Published in: Organic & biomolecular chemistry (2022)
The asymmetric synthesis of multisubstituted allylic amino acid derivatives was accomplished by the allylic alkylation of a chiral glycine-based nickel complex with vinylethylene carbonates. High enantioselectivities and diastereoselectivities were obtained under mild reaction conditions. The gram-scale synthesis was carried out with a good yield and high enantioselectivity, indicating that the method is a highly efficient route to chiral multisubstituted allylic amino acid derivatives.
Keyphrases
  • amino acid
  • highly efficient
  • capillary electrophoresis
  • ionic liquid
  • structure activity relationship
  • gram negative
  • reduced graphene oxide
  • carbon nanotubes
  • metal organic framework