Protonation Behavior of 1,1′-Bi-2-naphthol and Insights into Its Acid-Catalyzed Atropisomerization Научная публикация
Журнал |
Organic Letters
ISSN: 1523-7060 , E-ISSN: 1523-7052 |
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Вых. Данные | Год: 2017, Том: 19, Номер: 3, Страницы: 532-535 Страниц : 4 DOI: 10.1021/acs.orglett.6b03696 | ||||||
Ключевые слова | BINOL; MECHANISM; DFT | ||||||
Авторы |
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Организации |
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Информация о финансировании (1)
1 | Российский фонд фундаментальных исследований | 16-03-00357 |
Реферат:
The behavior of 1,1′-bi-2-naphthol (BINOL) in variety of (super)acid media has been studied by NMR. The results are combined with the theoretical (DFT) study of the role of mono- and diprotonated forms of BINOL in the acid-catalyzed atropisomerization of this compound. It is demonstrated that the process of enantiomeric configuration exchange proceeds mainly via internal rotation around the C1(sp3)–C1′(sp3) bond in intermediates such as C1-monoprotonated keto or C1,C1′-diprotonated forms of BINOL, depending on the acidity level.
Библиографическая ссылка:
Genaev A.M.
, Salnikov G.E.
, Shernyukov A.V.
, Zhu Z.
, Koltunov K.Y.
Protonation Behavior of 1,1′-Bi-2-naphthol and Insights into Its Acid-Catalyzed Atropisomerization
Organic Letters. 2017. V.19. N3. P.532-535. DOI: 10.1021/acs.orglett.6b03696 WOS Scopus РИНЦ CAPlusCA PMID OpenAlex
Protonation Behavior of 1,1′-Bi-2-naphthol and Insights into Its Acid-Catalyzed Atropisomerization
Organic Letters. 2017. V.19. N3. P.532-535. DOI: 10.1021/acs.orglett.6b03696 WOS Scopus РИНЦ CAPlusCA PMID OpenAlex
Даты:
Поступила в редакцию: | 12 дек. 2016 г. |
Опубликована online: | 17 янв. 2017 г. |
Опубликована в печати: | 3 февр. 2017 г. |
Идентификаторы БД:
Web of science: | WOS:000393539900027 |
Scopus: | 2-s2.0-85011340684 |
РИНЦ: | 29479011 |
Chemical Abstracts: | 2017:89109 |
Chemical Abstracts (print): | 166:165533 |
PMID (PubMed): | 28094529 |
OpenAlex: | W2572709642 |