The first synthesis and X-ray crystal structure of tetrahydropyrrolo[2,3-d]azocines

Tetrahydropyrrolo[3,2-c]pyridines (THPP) upon the reaction with DMAD in acetonitrile or DMSO at rt underwent ring expansion, affording tetrahydropyrrolo[2,3-d]azocines; these latter compounds have not previously been reported in the literature. The crystal structure and conformation of these derivatives was established by X-ray crystallography. © 2002 Published by Elsevier Science Ltd.

Авторы
Редакторы
-
Журнал
Издательство
Elsevier Ltd
Номер выпуска
38
Язык
Английский
Страницы
6767-6769
Статус
Опубликовано
Подразделение
-
Номер
-
Том
43
Год
2002
Организации
  • 1 Organic Chemistry Department, Russian Peoples Friendship University, 6, Miklukho-Maklayia St., Moscow 117198, Russian Federation
  • 2 N.S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Leninsky Prospekt 31, Moscow GSP-1 119991, Russian Federation
Ключевые слова
Azocine; Cleavage; Pyrrole; Ring expansion
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/168/