21306-38-7Relevant articles and documents
Double 1,3-Dipolar Cycloadditions of Meso-ionic Heterocycles to N-Substituted Maleimides
Nan'ya, Seiko,Kurachi, Yoshinori,Butsugan, Yasuo
, p. 1853 - 1855 (2007/10/02)
Double 1,3-dipolar cycloadditions of 2,4-diphenyl-3-methyloxazolium 5-oxide and 3-phenylsydnone to two molecules of N-substituted maleimide afforded one or two isomeric 4,8-iminobenzodipyrrole-1,3,5,7-tetrone derivatives owing to the types of heterocycles as well as N-substituents of maleimides.
CYCLOADDITION REACTION OF SYDNONE AND MALEIMIDE
Sun, Kwok Kun
, p. 317 - 320 (2007/10/02)
The cycloaddition of sydnone to maleimide afforded exclusively two isomeric 1:2-adducts.This bifunctional character of sydnone allows its reaction with bismaleimides to form novel polyimides.