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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2002 Volume 12, Issue 1, Pages 17–18 (Mi mendc4071)

This article is cited in 2 papers

Synthesis of 3-aryl-5,7-dinitrothiochromane 1,1-dioxides based on 2,4,6-trinitrotoluene

M. D. Dutov, O. V. Serushkina, S. A. Shevelev

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

Abstract: 3-Aryl-5,7-dinitrothiochromane 1,1-dioxides are formed by the condensation of methyl (2-methyl-3,5-dinitrobenzenesulfonyl)acetate and ethyl (2-methyl-3,5-dinitrobenzenesulfonyl)propionate, which are the products of 2,4,6-trinitrotoluene transformations, with aromatic aldehydes under conditions of the Knoevenagel reaction.

Language: English

DOI: 10.1070/MC2002v012n01ABEH001551



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