Stereoselective synthesis of highly functionalized (Z)-chloroalkene dipeptide isosteres containing an α,α-disubstituted amino acid

Abstract
Stereoselective synthesis of (Z)-chloroalkene dipeptide isosteres containing an α,α-disubstituted amino acid was realized from structurally unique tetra-substituted spirocyclic aziridines.
Funding Information
  • Japan Society for the Promotion of Science (20H03363)

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