Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/32987
Title: Synthesis of furan-3-carbonitriles by cyclization of cyano-substituted α,β-enones with potassium dinitromethanide
Authors: Demidov, O. P.
Демидов, О. П.
Keywords: Cyclization reactions;Michael reaction;Potassium dinitromethanide;α,β-enones
Issue Date: 2026
Publisher: Springer
Citation: Demidov M. R., Surkova T. V., Demidov O. P., Osyanin V. A., Klimochkin Y. N. Synthesis of furan-3-carbonitriles by cyclization of cyano-substituted α,β-enones with potassium dinitromethanide // Russian Chemical Bulletin. - 2026. - 75 (1). - pp. 251 - 259. - DOI: 10.1007/s11172-026-4882-9
Series/Report no.: Russian Chemical Bulletin
Abstract: A catalyst-free synthesis of furan-3-carbonitriles by cyclization of 2-arylidene-3-ketonitriles with potassium dinitromethanide was developed. Depending on the reagent ratio, this reaction afforded tri- and tetrasubstituted products. In the case of alkyl-substituted 2-arylidene-3-ketonitriles, the reaction diastereoselectively produced trans-5-nitro-4,5-dihydrofuran-3-carbonitriles.
URI: https://dspace.ncfu.ru/handle/123456789/32987
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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