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This article is cited in 21 scientific papers (total in 21 papers)
4,6-Dinitrobenzo[c]isothiazole: synthesis and 1,3-dipolar cycloaddition to azomethine ylide
L. S. Konstantinovaa, M. A. Bastrakova, A. M. Starosotnikova, I. V. Glukhovb, K. A. Lysova, O. A. Rakitina, S. A. Sheveleva a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Abstract:
1,3-Dipolar cycloaddition of 4,6-dinitrobenzo[c]isothiazole to (N-methyl-N-methylideneammonio)methanide (2 equiv.) gives 5,8-dimethyl-3b,6b-dinitrodecahydroisothiazolo[3,4-e]pyrrolo[3,4-g]isoindole, whose structure was confirmed by X-ray diffraction analysis.
Citation:
L. S. Konstantinova, M. A. Bastrakov, A. M. Starosotnikov, I. V. Glukhov, K. A. Lysov, O. A. Rakitin, S. A. Shevelev, “4,6-Dinitrobenzo[c]isothiazole: synthesis and 1,3-dipolar cycloaddition to azomethine ylide”, Mendeleev Commun., 20:6 (2010), 353–354
Linking options:
https://www.mathnet.ru/eng/mendc3091 https://www.mathnet.ru/eng/mendc/v20/i6/p353
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