Issue 2, 1989

The α-bromoester-imine condensation promoted by zinc-trimethylchlorosilane: a stereospecific short formal synthesis of (±)-carbapenem antibiotics and related compounds

Abstract

Ethyl bromoacetate reacts with imines in the presence of zinc activated by trimethylchlorosilane to give high yields of 3-unsubstituted β-lactams.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 74-76

The α-bromoester-imine condensation promoted by zinc-trimethylchlorosilane: a stereospecific short formal synthesis of (±)-carbapenem antibiotics and related compounds

F. P. Cossío, J. M. Odriozola, M. Oiarbide and C. Palomo, J. Chem. Soc., Chem. Commun., 1989, 74 DOI: 10.1039/C39890000074

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