Improved Method for Preparation of 3-(1H-Indol-3-yl)benzofuran-2(3H)-ones

3-(1H-Indol-3-yl)benzofuran-2(3H)-ones were efficiently accessed via polyphosphoric acid-mediated condensation of 3-(2-nitrovinyl)-1H-indoles with phenols. © 2022 by the authors. Licensee MDPI, Basel, Switzerland.

Авторы
Grishin I.Yu.1 , Arutiunov N.A.1 , Aksenov D.A. 1 , Aksenov N.A. 1 , Aksenov A.V. 1 , Gasanova A.Z.1 , Sorokina E.A. 2 , Lower C.3 , Rubin M. 1, 3
Журнал
Molecules
Издательство
MDPI AG
Номер выпуска
6
Язык
Английский
Статус
Опубликовано
Ссылка
Внешняя ссылка
DOI
10.3390/molecules27061902
Номер
1902
Том
27
Год
2022
Организации
  • 1 Department of Chemistry and Pharmacy, North Caucasus Federal University, 1a Pushkin St., Stavropol, 355017, Russian Federation
  • 2 Organic Chemistry Department, Peoples’ Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St., Moscow, 117198, Russian Federation
  • 3 Department of Chemistry, University of Kansas, 1567 Irving Hill Road, Lawrence, KS 66045, United States
Ключевые слова
Brønsted acid catalysis; cascade transformations; indoles; nitroalkanes; rearrangements
Дата создания
06.07.2022
Дата изменения
06.07.2022
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/83791/
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Статья
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