Issue 8, 1989

Tandem Michael addition–1,3-dipolar cycloaddition of imines of α-amino acid esters and aminoacetonitrile

Abstract

Four classes of new tandem Michael addition–1,3-dipolar cyclo-addition processes of imines of glycine methyl ester and amino acetonitrile are identified and examples of two classes which occur at 25 °C in acetonitrile in the presence of lithium salts and triethylamine, are reported.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 1550-1551

Tandem Michael addition–1,3-dipolar cycloaddition of imines of α-amino acid esters and aminoacetonitrile

D. A. Barr, G. Donegan and R. Grigg, J. Chem. Soc., Perkin Trans. 1, 1989, 1550 DOI: 10.1039/P19890001550

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