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4-R-7-Nitrobenzofurazans in [3+2] cycloaddition reactions with N-methylazomethine ylide

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Abstract

A number of new tetrahydroisoindole derivatives fused with the furazan ring were synthesized based on the 1,3-dipolar cycloaddition of N-methylazomethine ylide with substituted 4-nitrobenzofurazans. Substituents in the benzene ring were found to affect the cycloaddition process.

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Correspondence to A. M. Starosotnikov.

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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 73–75, January, 2012.

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Pechenkin, S.Y., Starosotnikov, A.M., Bastrakov, M.A. et al. 4-R-7-Nitrobenzofurazans in [3+2] cycloaddition reactions with N-methylazomethine ylide. Russ Chem Bull 61, 74–77 (2012). https://doi.org/10.1007/s11172-012-0011-z

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  • DOI: https://doi.org/10.1007/s11172-012-0011-z

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