Issue 20, 1994

Synthesis and transformations of 3-vinylcephalosporins. Part 6. Reactions of cephalosporin phosphoranes with bifunctional carbonyl compounds

Abstract

Cephalosporin C-3-phosphoranes have been converted into the corresponding 3-alkenylcephems and novel tricyclic derivatives on treatment with different bifunctional carbonyl compounds. The effect of substituents on the product ratio has been examined. The stereoselectivity of the ringclosure is explained on the basis of theoretical considerations.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1994, 3043-3046

Synthesis and transformations of 3-vinylcephalosporins. Part 6. Reactions of cephalosporin phosphoranes with bifunctional carbonyl compounds

J. Pitlik, T. E. Gunda, G. Batta and J. Jekö, J. Chem. Soc., Perkin Trans. 1, 1994, 3043 DOI: 10.1039/P19940003043

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