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1,3‐Dipolar cycloaddition of unstabilized N ‐methyl azomethine ylide to nitrobenzene annelated with azoles
Author(s) -
Starosotnikov Alexey M.,
Bastrakov Maxim A.,
Pechenkin Sergey Yu.,
Leontieva Margarita A.,
Kachala Vadim V.,
Shevelev Svyatoslav A.
Publication year - 2011
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.599
Subject(s) - chemistry , isoindole , azomethine ylide , cycloaddition , nitrobenzene , 1,3 dipolar cycloaddition , medicinal chemistry , organic chemistry , catalysis
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).