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Synthesis and structure of nitrocyclohexenylcarboxylates

The diene condensation of 3-nitro- and 3-bromo-3-nitroacrylates with 2,3-dimethyl-1,3-butadiene and isoprene obtained under the reaction condition from 3-methyl-3-thiolene-1,1-dioxide was investigated. The formed 6-nitro-3-cyclohexenylcarboxylates were subjected to the intramolecular transformation...

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Bibliographic Details
Published in:Russian journal of general chemistry 2011-09, Vol.81 (9), p.1845-1852
Main Authors: Anisimova, N. A., Kuzhaeva, A. A., Berkova, G. A., Berestovitskaya, V. M.
Format: Article
Language:English
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Summary:The diene condensation of 3-nitro- and 3-bromo-3-nitroacrylates with 2,3-dimethyl-1,3-butadiene and isoprene obtained under the reaction condition from 3-methyl-3-thiolene-1,1-dioxide was investigated. The formed 6-nitro-3-cyclohexenylcarboxylates were subjected to the intramolecular transformation (dehydration and dehydrohalogenation) to give the corresponding nitrocyclohexadienyl- and arylcarboxylates. The structure of the obtained compounds was established from the IR, 1 H NMR spectra and independent synthesis.
ISSN:1070-3632
1608-3350
DOI:10.1134/S1070363211090180