Transformations of N-acetyl(aroyl)-1-azafluorenium chlorides to give 9-α-hydroxyethylidene(arylidene)-1-azafluorenes

N-Acetyl (benzoyl)-1-azafluorenium chlorides were converted to 9-acetyl(benzoyl)-1-azafluorenes, which exist in the enol form, when they were treated with triethylamine in benzene in the presence of boron trifluoride etherate. The first step in the rearrangement is the conversion of the starting chlorides to N-acyl-substituted pseudoazulenes with subsequent N-C9 migration of the acyl group. © 1984 Plenum Publishing Corporation.

Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
8
Язык
Английский
Страницы
890-893
Статус
Опубликовано
Том
19
Год
1983
Организации
  • 1 Patrice Lumumba Peoples' Friendship University, Moscow, 117923, Russian Federation
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/1413/