Three-component synthesis of 5,6-dihydropyrrolo[2,1-a]isoquinolines from 1-aroyl-3,4-dihydroisoquinolines, electron-deficient alkynes and NH-acids

The three-component domino reaction involving 1-aroyl-3,4-dihydroisoquinolines, terminal alkynes, and cyclic NH-acids is a new method for the synthesis of 5,6-dihydropyrrolo[2,1-a]isoquinolines containing in position 3, cyclic nitrogen-containing fragments. The transformation is performed under microwave irradiation in dry acetonitrile at 130 °C. © 2022 Elsevier Ltd

Авторы
Miftyakhova A.R. , Sidakov M.B. , Borisova T.N. , Ilyushenkova V.V. , Fakhrutdinov A.N. , Sorokina E.A. , Varlamov A.V. , Voskressensky L.G.
Журнал
Издательство
Elsevier Ltd
Язык
Английский
Статус
Опубликовано
Номер
153991
Том
103
Год
2022
Организации
  • 1 Organic Chemistry Department, Peoples’ Friendship, University of Russia (RUDN University), 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation
  • 2 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Prosp., Moscow, 119991, Russian Federation
Ключевые слова
Domino reaction; NH-acids; Pyrrolo[2,1-a]isoquinolines; Terminal alkynes; Three-component reactions
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