Hydrogen-free reductive amination using iron pentacarbonyl as a reducing agent

We developed solvent-free reductive amination without an external hydrogen source using iron pentacarbonyl as a reducing agent. Neither a catalyst nor any other additives were employed. Various types of substrates are suitable for the reaction, including those with low reactivity, e.g. benzophenone. Among others, the protocol tolerates bromo-, cyano-, benzyloxy-, pyrimidyl and styryl moieties. © 2017 The Royal Society of Chemistry.

Авторы
Afanasyev O.I.1 , Usanov D.L.2 , Chusov D. 1, 3
Издательство
Royal Society of Chemistry
Номер выпуска
48
Язык
Английский
Страницы
10164-10166
Статус
Опубликовано
Том
15
Год
2017
Организации
  • 1 A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Vavilova St 28, Moscow, 119991, Russian Federation
  • 2 Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, MA 02138, United States
  • 3 Faculty of Science, RUDN University, 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation
Ключевые слова
Chemistry; Positive ions; Hydrogen sources; Iron pentacarbonyls; Reductive amination; Solvent free; Amines
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/6142/
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