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Oxidative Rearrangement of 2‐(2‐Aminobenzyl)furans: Synthesis of Functionalized Indoles and Carbazoles Full article

Journal European Journal of Organic Chemistry
ISSN: 1434-193X , E-ISSN: 1099-0690
Output data Year: 2021, Volume: 2021, Number: 8, Pages: 1274-1285 Pages count : 12 DOI: 10.1002/ejoc.202001608
Authors Merkushev Anton A. 1 , Makarov Anton S. 1 , Shpuntov Pavel M. 2 , Abaev Vladimir T. 3,4 , Trushkov Igor V. 5,6 , Uchuskin Maxim G. 1
Affiliations
1 Perm State University, Bukireva st. 15, Perm 614990 Russian Federation
2 Kuban State Technological University Moskovskaya St. 2 Krasnodar 350072 Russian Federation
3 North Caucasus Federal University Pushkin St. 1a Stavropol 355009 Russian Federation
4 North-Ossetian State University Vatutina St. 46 Vladikavkaz 362025 Russian Federation
5 D. Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Samory Mashela St. 1, Moscow, 117997 Russian Federation
6 N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky Pr. 47, Moscow, 119991 Russian Federation

Abstract: 2-(2-Acylvinyl)indoles obtained by oxidative rearrangement of substituted 2-(2-aminobenzyl)furans could be used to construct structural analogues of antifungal alkaloids caulindoles A−D as well as other indole-derived molecules and substituted carbazoles by introducing new reaction centers into the structure of starting materials or by synthetic manipulation with functional groups of the obtained compounds.
Cite: Merkushev A.A. , Makarov A.S. , Shpuntov P.M. , Abaev V.T. , Trushkov I.V. , Uchuskin M.G.
Oxidative Rearrangement of 2‐(2‐Aminobenzyl)furans: Synthesis of Functionalized Indoles and Carbazoles
European Journal of Organic Chemistry. 2021. V.2021. N8. P.1274-1285. DOI: 10.1002/ejoc.202001608 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000616355500001
Scopus: 2-s2.0-85100821371
OpenAlex: W3127915001
Citing:
DB Citing
OpenAlex 12
Scopus 12
Web of science 11
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