Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/5437
Title: Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangement
Authors: Demidov, O. P.
Демидов, О. П.
Keywords: 2-naphthol;Betti reaction;Boric acid;Carbo-Piancatelli rearrangement;Furfural;Multicomponent reaction
Issue Date: 2019
Publisher: Springer New York LLC
Citation: Gutnov, A.V., Abaev, V.T., Demidov, O.P. Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangement // Chemistry of Heterocyclic Compounds. - 2019. - Volume 55. - Issue 3. - Pages 280-282
Series/Report no.: Chemistry of Heterocyclic Compounds
Abstract: Condensation of 2-naphthol, furfural, and acetamide in the presence of boric acid as acidic catalyst has led to Betti product N-[furan-2-yl(2-hydroxynaphthalen-1-yl)methyl]acetamide along with a new 10,10-dihydrocyclopenta[b]naphtho[1,2-d]furan derivative, which resulted from rare carbo-Piancatelli rearrangement. The structure is confirmed by 1 H, 13 C NMR, HRMS, and X-ray analyses. Mechanism of the transformation is discussed
URI: http://hdl.handle.net/20.500.12258/5437
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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