[Figure not available: see fulltext.] The reactions of 2-benzylidene-3-methyl-4-nitro-2,5-dihydrothiophene 1,1-dioxides with dimedone were used to synthesize a series of tricyclic compounds containing fused nitrosulfolane and octahydrochromenone rings. The structural features of the obtained polycyclic compounds were established on the basis of IR and NMR spectra, as well as X-ray structural analysis.

Original languageEnglish
Pages (from-to)58-63
Number of pages6
JournalChemistry of Heterocyclic Compounds
Volume58
Issue number1
DOIs
StatePublished - Jan 2022

    Scopus subject areas

  • Organic Chemistry

    Research areas

  • 2-benzylidene-3-methyl-4-nitro-2,5-dihydrothiophene 1,1-dioxides, enolizable cyclic СН acids, sulfolenes, tandem process

ID: 98952836