Improved method for preparation of 3-(1H-Indol-3-yl)benzofuran-2(3H)-ones

Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/19401

Title:	Improved method for preparation of 3-(1H-Indol-3-yl)benzofuran-2(3H)-ones
Authors:	Grishin, I. Y. Гришин, И. Ю. Arutiunov, N. A. Арутюнов, Н. А. Aksenov, D. A. Аксенов, Д. А. Aksenov, N. A. Аксенов, Н. А. Aksenov, A. V. Аксенов, А. В. Gasanova, A. Z. Гасанова, А. З. Rubin, M. A. Рубин, М. А.
Keywords:	Brønsted acid catalysis;Nitroalkanes;Rearrangements;Indoles;Cascade transformations
Issue Date:	2022
Publisher:	MDPI
Citation:	Grishin, I. Yu., Arutiunov, N. A., Aksenov, D. A., Aksenov, N. A., Aksenov, A. V., Gasanova, A. Z., Sorokina, E. A., Lower, C., Rubin, M. Improved method for preparation of 3-(1H-Indol-3-yl)benzofuran-2(3H)-ones // Molecules. - 2022. - Том 27. - Выпуск 6. - Номер статьи 1902. - DOI10.3390/molecules27061902
Series/Report no.:	Molecules
Abstract:	3-(1H-Indol-3-yl)benzofuran-2(3H)-ones were efficiently accessed via polyphosphoric acid-mediated condensation of 3-(2-nitrovinyl)-1H-indoles with phenols.
URI:	http://hdl.handle.net/20.500.12258/19401
Appears in Collections:	Статьи, проиндексированные в SCOPUS, WOS

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