Cyanoethylation of azafluorenes and syntheses of alcohols containing an azafluorene fragment

Isomeric (with respect to the position of the nitrogen atom) azafluorenes were cyanoethylated. The resulting 9,9-bis(β-cyanoethyl) derivatives were converted to the corresponding dibasic acids and their diesters. The latter were subjected to the Dieckmann reaction to obtain spiro compounds with azafluorene and cyclohexene fragments. The analogous spirans with 1,3-dioxalane and 1,3-dioxane rings were obtained from 3-methyl-2-azafluorenone. © 1983 Plenum Publishing Corporation.

Редакторы
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Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
12
Язык
Английский
Страницы
1290-1294
Статус
Опубликовано
Подразделение
-
Номер
-
Том
18
Год
1982
Организации
  • 1 Patrice Lumumba People's Friendship University, Moscow, 117923, Russian Federation
Ключевые слова
-
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/1441/