Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/19606
Title: One-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitriles
Authors: Aksenov, N. A.
Аксенов, Н. А.
Aksenov, A. V.
Аксенов, А. В.
Kurenkov, I. A.
Куренков, И. А.
Kirilov, N. K.
Кирилов, Н. К.
Aksenov, D. A.
Аксенов, Д. А.
Arutiunov, N. A.
Арутюнов, Н. А.
Aksenova, D. S.
Аксенова, Д. С.
Rubin, M. A.
Рубин, М. А.
Keywords: Brønsted acid catalysis;Cascade transformations;Indoles;Nitroalkanes;Rearrangements
Issue Date: 2022
Publisher: MDPI
Citation: Aksenov, N. A., Aksenov, A. V., Kurenkov, I. A., Kirillov, N. K., Aksenov, D. A., Arutiunov, N. A., Aksenova, D. S., Rubin, M. One-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitriles // Molecules. - 2022. - Том 27. - Выпуск 9. - Номер статьи 2808. - DOI10.3390/molecules27092808
Series/Report no.: Molecules
Abstract: A highly efficient and expeditious one-pot approach towards 2-(3-oxoindolin-2-yl)acetonitriles was designed, which involves a base-assisted aldol reaction of ortho-nitroacetophenones, followed by hydrocyanation, triggering an unusual reductive cyclization reaction.
URI: http://hdl.handle.net/20.500.12258/19606
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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