Highly stereocontrolled synthesis of a novel tribactam by reaction of an ester enolate with a N-trimethylsilylimine

This publication has 23 references indexed in Scilit:

• A Three Component Coupling Approach to a Chiral 1.beta.-Methylcarbapenem Key Intermediate
  The Journal of Organic Chemistry, 1995
• The ester enolate-imine condensation route to .beta.-lactams
  Chemical Reviews, 1989
• Synthetic studies of 1-.BETA.-methylcarbapenem antibiotics.
  The Journal of Antibiotics, 1989
• A new approach to the chiral synthesis of the 1-.beta.-methylcarbapenem key precursor using an achiral ketone Sn(II) enolate
  The Journal of Organic Chemistry, 1987
• Practical Synthesis of (3R,4R)-4-Acetoxy-3-[1(R)-t-Butyldimethylsilyloxyethyl]Aze-Tidin-2-One. A Key Intermediate for Penem and Carbapenem Synthesis
  Synthetic Communications, 1987
• Enantioselective Syntheses of Carbapenem Antibiotics
  HETEROCYCLES, 1987
• Recent Developments in the Field of β‐Lactam Antibiotics
  Angewandte Chemie International Edition in English, 1985
• Synthetic Carbapenem Antibiotics. I. 1-b-Methylcarbapenem
  HETEROCYCLES, 1984
• Synthesis of Carbapenem Antibiotics
  HETEROCYCLES, 1982
• 2-(Alkylthio)penem-3-carboxylic acids. IV. Synthesis of (hydroxyethyl)azetidinone precursors to 1-thia analogs of thienamycin.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1981