Product structure in the reaction of dimethyl acetylenedicarboxylate with 2-furyl-1,2,3,4-tetrahydroquinolines

Dimethyl acetylenedicarboxylate reacts with 4-substituted and 3,4-fused 2-furyl-1,2,3,4-tetrahydroquinoline derivatives at the furan fragment according to the [4 + 2]-cycloaddition pattern. The reaction is not stereoselective, and it yields two diastereoisomeric 7-oxabicyclo[2.2.1]hepta-2,5-dienes whose structure was determined by X-ray analysis and NMR spectroscopy. © 2007 Pleiades Publishing, Ltd.

Авторы
Zubkov F.I. 1 , Zaitsev V.P. 1 , Orlova A.A. 1 , Peregudov A.S.2 , Mikhailova N.M. 1 , Varlamov A.V. 1
Номер выпуска
8
Язык
Английский
Страницы
1202-1208
Статус
Опубликовано
Том
43
Год
2007
Организации
  • 1 Russian University of Peoples' Friendship, ul. Miklukho-Maklaya 6, Moscow 117198, Russian Federation
  • 2 Nesmeyanov Institute of Organometallic Compounds, Russian Academy of Sciences, Moscow, Russian Federation
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/3220/