Unexpected reductive transformation of 1-substituted 5-hydroxy-4,5-diphenyl-1H-imidazol-2(5H)-ones and their cyclic analogs by the reaction with thiourea and hydrochloric acid

An unexpected reductive transformation of 1-substituted 5-hydroxy-4,5-diphenyl-1H-imidazol-2(5H)-ones (imidazolones) and their cyclic analogs to give 1-substituted 4,5-diphenyl-1H-imidazol-2(5H)-ones (imidazolinones) upon reaction with thiourea and hydrochloric acid was discovered. © 2017 Elsevier Ltd

Авторы
Baranov V.V. 1, 2 , Antonova M.M.1 , Karnoukhova V.A.3 , Kravchenko A.N.1
Журнал
Tetrahedron Letters
Издательство
Elsevier Ltd
Номер выпуска
23
Язык
Английский
Страницы
2203-2205
Статус
Опубликовано
Ссылка
Внешняя ссылка
DOI
10.1016/j.tetlet.2017.04.061
Том
58
Год
2017
Организации
  • 1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., Moscow, 119991, Russian Federation
  • 2 Peoples’ Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya St., Moscow, 117198, Russian Federation
  • 3 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilova St., Moscow, 119991, Russian Federation
Ключевые слова
Heterocycles; Imidazolinones; Imidazolones; Reductive transformation; Thiourea
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/6063/
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Статья
Anh L.T., Titov A.A., Kobzev M.S., Voskressensky L.G., Varlamov A.V., Dorovatovskii P.V., Khrustalev V.N.
Acta Crystallographica Section E: Crystallographic Communications. International Union of Crystallography. Том 73. 2017. С. 1770-1773