JOURNAL of the Tunisian Chemical Society

serving the Research, the Education and the Industry

Stéréochimie de la réaction des iminoesters vis-à-vis du système chlorure d'acide / triéthylamine. Interprétation théorique qualitative

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The stereochemistry of acids halide and iininoesters is studied. A qualitative molecular orbital interpretation is suggested to explain the stereochemistry of the resulting β-lactams. Stereoselectivity of the reaction is directly related to the stability of the supposed intermediate.

D.A. Sidhoum, A. Krallafa, H. Benhaoua

Stereochemistry, β-lactams, Stereoselectivity, Diastereoselectivity, Molecular Orbitals

Pages 13-16

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