Abstract
The 1,3-dipolar cycloaddition of unstabilized azomethine ylide 1 with meta-dinitrobenzene fused with nitrogen heterocycles affords the corresponding decahydropyrrolo[3,4-e]isoindole cycloadducts in good yields. This is a first example of [3+2]-cycloaddition of azomethine ylides to nitroarenes. © 2010 HeteroCorporation.
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APA
Bastrakov, M. A., Starosotnikov, A. M., Pechenkin, S. Y., Kachala, V. V., Glukhov, I. V., & Shevelev, S. A. (2010). Double 1,3-dipolar cycloaddition of N-methyl azomethine ylide to meta-dinitrobenzene annelated with nitrogen aromatic heterocycles. Journal of Heterocyclic Chemistry, 47(4), 893–896. https://doi.org/10.1002/jhet.423
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