Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/23336
Title: A sequence of acylamination and acylation reactions in polyphosphoric acid – a novel approach to the Friedländer synthesis of 2-arylquinolines
Authors: Grishin, I. Y.
Гришин, И. Ю.
Malyuga, V. V.
Малюга, В. В.
Aksenov, D. A.
Аксенов, Д. А.
Kirilov, N. K.
Кирилов, Н. К.
Ovcharov, S. N.
Овчаров, С. Н.
Sarapii, A. V.
Сарапий, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Aksenov, A. V.
Аксенов, А. В.
Keywords: Polyphosphoric acid;One-pot synthesis;Nitro compounds;Quinolines;Acylamination
Issue Date: 2022
Citation: Grishin, I.Y., Malyuga, V.V., Aksenov, D.А., Kirilov, N.K., Abakarov, G.M., Ovcharov, S.N., Sarapii, A.V., Aksenov, N.А., Aksenov, A.V. A sequence of acylamination and acylation reactions in polyphosphoric acid – a novel approach to the Friedländer synthesis of 2-arylquinolines // Chemistry of Heterocyclic Compounds. - 2022. - 58 (6-7), pp. 313-318. - DOI: 10.1007/s10593-022-03090-x
Series/Report no.: Chemistry of Heterocyclic Compounds
Abstract: A method for the synthesis of 2-(2-acylaminoaryl)quinolines was developed based on a one-pot sequence of direct electrophilic acylamination of arenes with nitroalkanes in polyphosphoric acid and acylation at the ortho position with respect to the acylamino group.
URI: http://hdl.handle.net/20.500.12258/23336
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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