Issue 10, 1990

Chemistry of O-silylated ketene acetals: a stereoselective synthesis of chiral thienamycin intermediate

Abstract

A stereoselective synthesis of chiral thienamycin intermediate (10) involving a diastereoselective Michael addition and a silicon-induced Pummerer-type reaction is described.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 727-729

Chemistry of O-silylated ketene acetals: a stereoselective synthesis of chiral thienamycin intermediate

Y. Kita, N. Shibata, T. Miki, Y. Takemura and O. Tamura, J. Chem. Soc., Chem. Commun., 1990, 727 DOI: 10.1039/C39900000727

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