Allylation and heterocycloaddition reactions of aldimines: Furan- and quinolinecarboxaldehydes

New derivatives of α-substituted furans were prepared in high yields from easily available α-furfurylidenbenzilamines via nucleophilic C-allylation. The homoallylamines obtained this way were used for the synthesis of some polyfunctional aminobutene derivatives. In addition, 4-thiazolidinones some of which are hetaryl substituted at the 2-position were prepared by the reaction of mercapto acids with quinoline carboxaldehydes and p-phenetidine. All new products were fully characterized.

Авторы
Kouznetsov V.2 , Öcal N.1 , Turgut Z.1 , Zubkov F. 3 , Kaban S.1 , Varlamov A.V. 3
Редакторы
-
Журнал
Издательство
Springer Wien
Номер выпуска
6-7
Язык
Английский
Страницы
671-677
Статус
Опубликовано
Подразделение
-
Номер
-
Том
129
Год
1998
Организации
  • 1 Yildiz Technical University, Department of Chemistry, 80270 Sisli, Istanbul, Turkey
  • 2 School of Chemistry, Industrial University of Santander, Bucaramanga, Colombia
  • 3 Department of Organic Chemistry, Russ. Peoples Friendship University, Moscow 117923, Russian Federation
Ключевые слова
4-Thiazolidinone; Diels-Alder adduct; Nitrone; α-Furfurylidenbenzilamine; α-Substituted furan
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/688/