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Synthesis and some properties of 2H-benzimidazole 1,3-dioxides Full article

Journal Tetrahedron
ISSN: 0040-4020
Output data Year: 2015, Volume: 71, Number: 39, Pages: 7233-7244 Pages count : 12 DOI: 10.1016/j.tet.2015.03.096
Tags Benzofuroxan; 2H-benzimidazole 1,3-dioxide; 3H-[2,1,4]benzoxadiazine 4-oxide; Thermal transformations; Photochromic compounds
Authors Chugunova Elena 1 , Samsonov Vladimir 2 , Gerasimova Tatiana 2 , Rybalova Tatiana 2,3 , Bagryanskaya Irina 2,3
Affiliations
1 A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center, Russian Academy of Sciences, 8 Arbuzov St., 420088, Kazan, Russia
2 N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9 Prosp, Akad. Lavrentґeva, 630090, Novosibirsk, Russia
3 Novosibirsk State University, Pirogova Str. 2, 630090, Novosibirsk, Russia

Abstract: The synthesis of novel 2H-benzimidazole 1,3-dioxides on the basis of benzofuroxans interaction with alcohols in acids is described. The formation of a stable secondary carbocation from alcohol is necessary for formation of 2H-benzimidazole 1,3-dioxide while substituents in benzofuroxans don't prevent the reaction. Under heating 2H-benzimidazole 1,3-dioxides are rearranged to 3H-[2,1,4]benzoxadiazine 4-oxides whose stability depends on substituents in the aromatic ring. Under irradiation oxadiazines are converted back to 2H-benzimidazole 1,3-dioxides. (C) 2015 Elsevier Ltd. All rights reserved.
Cite: Chugunova E. , Samsonov V. , Gerasimova T. , Rybalova T. , Bagryanskaya I.
Synthesis and some properties of 2H-benzimidazole 1,3-dioxides
Tetrahedron. 2015. V.71. N39. P.7233-7244. DOI: 10.1016/j.tet.2015.03.096 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Sep 1, 2015
Identifiers:
Web of science: WOS:000360511000018
Scopus: 2-s2.0-84939258700
Elibrary: 24509227
OpenAlex: W2327005696
Citing:
DB Citing
Web of science 14
Scopus 16
Elibrary 14
OpenAlex 15
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