Abstract
Cycloadditions of benzonaphthyridines, their N-oxides and ylides from their quaternary salts are presented. Dimethylacetylenedicarboxylate, diethyl maleate, acrylonitrile and others were used as dipolarophiles. Cyclization of N-phenacylbenzonaphthyridinium bromides with ammonium acetate as well as vicarious substitution of hydrogen of benzonaphthyridine N-oxides are also reported and pathways to their formation are proposed.
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CITATION STYLE
APA
Bachowska, B., & Zujewska, T. (2001). Chemistry and applications of benzonaphthyridines. Arkivoc, 2001(6), 77–84. https://doi.org/10.3998/ark.5550190.0002.607
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