Issue 8, 1986

Iminium ion route to azomethine yields from primary and secondary amines

Abstract

Iminium ion formation between primary or secondary amines and carbonyl compounds containing the moiety O[double bond, length half m-dash]C–C[double bond, length half m-dash]X results in a facile and stereospecific generation of azomethine yields which can be trapped in 1,3-dipolar cycloaddition reactions.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 602-604

Iminium ion route to azomethine yields from primary and secondary amines

H. Ardill, R. Grigg, V. Sridharan, S. Surendrakumar, S. Thianpatanagul and S. Kanajun, J. Chem. Soc., Chem. Commun., 1986, 602 DOI: 10.1039/C39860000602

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