Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/5437
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dc.contributor.authorDemidov, O. P.-
dc.contributor.authorДемидов, О. П.-
dc.date.accessioned2019-05-20T13:34:47Z-
dc.date.available2019-05-20T13:34:47Z-
dc.date.issued2019-
dc.identifier.citationGutnov, 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 280-282ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/5437-
dc.description.abstractCondensation 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 discussedru
dc.language.isoenru
dc.publisherSpringer New York LLCru
dc.relation.ispartofseriesChemistry of Heterocyclic Compounds-
dc.subject2-naphtholru
dc.subjectBetti reactionru
dc.subjectBoric acidru
dc.subjectCarbo-Piancatelli rearrangementru
dc.subjectFurfuralru
dc.subjectMulticomponent reactionru
dc.titleBetti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangementru
dc.typeСтатьяru
vkr.amountPages 280-282ru
vkr.instИнститут математики и естественных наук-
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