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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2012 Volume 22, Issue 1, Pages 35–36 (Mi mendc2729)

This article is cited in 6 papers

Synthesis of fused isoindoles via 1,3-dipolar cycloaddition of 1,3-oxazolium-5-olates (münchnones) with nitro benzazoles

S. Yu. Pechenkin, A. M. Starosotnikov, M. A. Bastrakov, V. V. Kachala, S. A. Shevelev

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: 1,3-Dipolar cycloaddition of 1,3-oxazolium-5-olates at benzazoles nitrated at the benzene ring affords the corresponding azoloisoindole derivatives.

Keywords: 1,3-dipolar cycloaddition, benzoazoles, isoindoles, 1,3-oxazolium5-olates, nito compounds.

Language: English

DOI: 10.1016/j.mencom.2012.01.013



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