作者: Shu-Li You , Jeffery W. Kelly
DOI: 10.1021/OL049439C
关键词:
摘要: A highly efficient enantiospecific synthesis of imidazoline-based amino acids is reported from dipeptides composed a C-terminal β-amino-α-amino acid residue using bis(triphenyl) oxodiphosphonium trifluoromethanesulfonate. These imidazolines were easily converted to imidazoles and incorporated into macrolactam analogues bistratamide H without loss stereochemical integrity.