
%0 Journal Article
%A Matusiak, Grazyna 
%T 1,3-Dipolar Cycloaddition Reactions of the Ylide Derived from 6-Phenacyl-benzo[<emph type="2">f</emph>][1,7]naphthyridinium Bromide
%J Australian Journal of Chemistry
%D 1999/02/19
%V 52
%N 2
%P 149-152
%K 
%R https://doi.org/10.1071/C98109
%U https://www.publish.csiro.au/paper/C98109 
%X The 1,3-dipolar cycloaddition reactions of 4,6-diazaphenanthrene 6-phenacylide formed in situ from the quaternary 6-phenacylbenzo&#91;f&#93;&#91;1,7&#93;naphthyridinium bromide in basic medium were examined; methacrylic acid, methyl methacrylate, butyl vinyl ether, methyl vinyl ketone, maleic anhydride and dimethyl acetylenedicarboxylate were used as the dipolarophiles. 
