Stereoselective synthesis of β-lactams

This publication has 11 references indexed in Scilit:

• Preparation of chiral 3-unsubstituted β-lactams from 3-hydroxy β-lactams by using the alkoxyketene-imine cycloaddition reaction as an approach to the azetidinone ring: A formal synthesis of the carbapenem antibiotic (+)-PS-5.
  Tetrahedron Letters, 1991
• Asymmetric synthesis of 1,3,4-trisubstituted and 3,4-disubstituted 2-azetidinones: strategy based on use ofD-glucosamine as a chiral auxiliary in the Staudinger reaction
  Journal of the Chemical Society, Perkin Transactions 1, 1990
• Studies on lactams. 81. Enantiospecific synthesis and absolute configuration of substituted .beta.-lactams from D-glyceraldehyde acetonide
  The Journal of Organic Chemistry, 1988
• Cycloadditions of cyanoketenes to cinnamylidenamines and benzylidenamines. Synthetic scope, stereochemistry, and mechanism
  The Journal of Organic Chemistry, 1985
• Total synthesis of (.+-.)-3-deoxy-D-manno-2-octulopyranosate
  Journal of the American Chemical Society, 1985
• Syntheses of β-lactams from acetic acids and imines induced by phenyl dichlorophosphate reagent
  Tetrahedron, 1985
• A series of (2S)-2-O-protected-2-hydroxypropanals (L-lactaldehydes) suitable for use as optically active intermediates
  The Journal of Organic Chemistry, 1983
• An Enantioselective β‐Lactam Synthesis Starting from L‐(S)‐Glyceraldehyde Acetonide
  Helvetica Chimica Acta, 1983
• A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compounds
  The Journal of Organic Chemistry, 1981
• A convenient synthesis of α-amino-β-lactams
  Tetrahedron, 1981