Transformations of cotarnine chloride by the action of silver acetylides and alkynes

Three-component reactions of cotarnine chloride with silver acetylides and methyl propiolate or ethynyl methyl ketone in acetonitrile, as well as two-component reactions of 5-phenylethynyl-substituted tetrahydro[1,3]dioxolo[4,5-g]isoquinoline with alkynes in various solvents were studied. Performing them in 2,2,2-trifluoroethanol as the solvent, 10-phenylethynyl-substituted tetrahydro[1,3]dioxolo[4,5-i]-[3]benzazocines were obtained in good yields. © 2016 Springer Science+Business Media New York.

Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
5
Язык
Английский
Страницы
316-321
Статус
Опубликовано
Том
52
Год
2016
Организации
  • 1 Peoples' Friendship University of Russia, 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation
Ключевые слова
Cotarnine chloride; DMAD; Ethynyl methyl ketone; Methyl propiolate; Silver acetylides; [1,3]dioxolo[4,5-g]pyrrolo[2,1-a]isoquinolines; [1,3]dioxolo[4,5-i][3]benzazocines
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