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1,3-Dipolar cycloaddition of unstabilized N-methyl azomethine ylide to nitrobenzene annelated with azoles

✍ Scribed by Alexey M. Starosotnikov; Maxim A. Bastrakov; Sergey Yu. Pechenkin; Margarita A. Leontieva; Vadim V. Kachala; Svyatoslav A. Shevelev

Publisher: Journal of Heterocyclic Chemistry
Year: 2011
Tongue: English
Weight: 124 KB
Volume: 48
Category: Article
ISSN: 0022-152X
DOI: 10.1002/jhet.599

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✦ Synopsis

Abstract

The 1,3‐dipolar cycloaddition of unstabilized N‐methyl azomethine ylide to mononitro benzazoles was studied. Depending on the nature of substituents and annelated azoles, the reaction affords previously unknown isoindole fused heterocyclic systems. The reactivity of the cycloadducts was examined. J. Heterocyclic Chem., (2011).

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