Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangement

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...

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Главные авторы:	Demidov, O. P., Демидов, О. П.
Формат:	Статья
Язык:	English
Опубликовано:	Springer New York LLC 2019
Темы:	2-naphthol Betti reaction Boric acid Carbo-Piancatelli rearrangement Furfural Multicomponent reaction
Online-ссылка:	https://dspace.ncfu.ru/handle/20.500.12258/5437
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spelling	ir-20.500.12258-54372025-02-13T12:56:52Z Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangement Demidov, O. P. Демидов, О. П. 2-naphthol Betti reaction Boric acid Carbo-Piancatelli rearrangement Furfural Multicomponent reaction 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 2019-05-20T13:34:47Z 2019-05-20T13:34:47Z 2019 Статья 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 http://hdl.handle.net/20.500.12258/5437 en Chemistry of Heterocyclic Compounds application/pdf application/pdf Springer New York LLC
institution	СКФУ
collection	Репозиторий
language	English
topic	2-naphthol Betti reaction Boric acid Carbo-Piancatelli rearrangement Furfural Multicomponent reaction
spellingShingle	2-naphthol Betti reaction Boric acid Carbo-Piancatelli rearrangement Furfural Multicomponent reaction Demidov, O. P. Демидов, О. П. Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangement
description	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
format	Статья
author	Demidov, O. P. Демидов, О. П.
author_facet	Demidov, O. P. Демидов, О. П.
author_sort	Demidov, O. P.
title	Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangement
title_short	Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangement
title_full	Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangement
title_fullStr	Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangement
title_full_unstemmed	Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangement
title_sort	betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-piancatelli rearrangement
publisher	Springer New York LLC
publishDate	2019
url	https://dspace.ncfu.ru/handle/20.500.12258/5437
work_keys_str_mv	AT demidovop bettireactionof2naphtholfurfuralandacetamideanunexpectedcaseofsecondarycarbopiancatellirearrangement AT demidovop bettireactionof2naphtholfurfuralandacetamideanunexpectedcaseofsecondarycarbopiancatellirearrangement
_version_	1842245485821165568

Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-Piancatelli rearrangement

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