Please use this identifier to cite or link to this item:
https://dspace.ncfu.ru/handle/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 |
Files in This Item:
File | Size | Format | |
---|---|---|---|
scopusresults 2174 .pdf Restricted Access | 1.75 MB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.