Reaction of N-cyclohexyl-2-(2-hydroxynaphthalen-1-yl)pyrrolidine-1-carboxamide with resorcinol and its derivatives and synthesis of polyphenols
- Autores: Smolobochkin A.V.1, Gazizov A.S.1, Burilov A.R.1, Pudovik M.A.1
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Afiliações:
- A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center of the Russian Academy of Sciences
- Edição: Volume 65, Nº 5 (2016)
- Páginas: 1377-1379
- Seção: Brief Communications
- URL: https://journals.rcsi.science/1066-5285/article/view/238354
- DOI: https://doi.org/10.1007/s11172-016-1465-1
- ID: 238354
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Resumo
An acid-catalyzed pyrrolidine ring opening in 2-(2-hydroxynaphthalen-1-yl)pyrrolidine-1-carboxamides in the presence of resorcinols furnished new calix[4]resorcinols or 1,1-diarylbutanes modified with urea fragments. The process follows the retro-Mannich reaction mechanism, with the 2-naphthol fragment playing the role of the leaving group.
Sobre autores
A. Smolobochkin
A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center of the Russian Academy of Sciences
Email: agazizov@iopc.ru
Rússia, 8 ul. Akad. Arbuzova, Kazan, 420088
A. Gazizov
A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center of the Russian Academy of Sciences
Autor responsável pela correspondência
Email: agazizov@iopc.ru
Rússia, 8 ul. Akad. Arbuzova, Kazan, 420088
A. Burilov
A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center of the Russian Academy of Sciences
Email: agazizov@iopc.ru
Rússia, 8 ul. Akad. Arbuzova, Kazan, 420088
M. Pudovik
A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center of the Russian Academy of Sciences
Email: agazizov@iopc.ru
Rússia, 8 ul. Akad. Arbuzova, Kazan, 420088
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