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Transformations of 2,2-dimethyl-2,4-dihydro-3H-pyrrol-3-on-1-oxide derivatives in the Vilsmeier-Haack reaction conditions Full article

Journal Tetrahedron
ISSN: 0040-4020
Output data Year: 2008, Volume: 64, Number: 39, Pages: 9191-9196 Pages count : DOI: 10.1016/j.tet.2008.07.070
Tags nitrogen heterocycles; rearrangement; 1-Hydroxy-1,2-dihydro-3H-pyrrol-3-one; Vilsmeier-Haack reaction
Authors Becker Christina , Roshchupkina Galina , Rybalova Tatyana , Gatilov Yuri , Reznikov Vladimir
Affiliations
1 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia
2 (Данные Web of science) Russian Acad Sci, NN Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia

Abstract: Enhydroxylaminones-2,2-dimethyl-2,4-dihydro-3H-pyrrol-3-on-1-oxides were shown to give various chlorinated products in the Vilsmeier-Haack reaction. The general sequence of the reaction steps is determined and the extent of the reaction was shown to be strongly dependent oil the substrate structure. (C) 2008 Elsevier Ltd. All rights reserved.
Cite: Becker C. , Roshchupkina G. , Rybalova T. , Gatilov Y. , Reznikov V.
Transformations of 2,2-dimethyl-2,4-dihydro-3H-pyrrol-3-on-1-oxide derivatives in the Vilsmeier-Haack reaction conditions
Tetrahedron. 2008. V.64. N39. P.9191-9196. DOI: 10.1016/j.tet.2008.07.070 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Sep 1, 2008
Identifiers:
Web of science: WOS:000259650200003
Scopus: 2-s2.0-49149118123
Elibrary: 13589504
OpenAlex: W2094010915
Citing:
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Web of science 5
Scopus 5
Elibrary 5
OpenAlex 8
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