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Enhanced enantiostability of BINOL dimethyl ether under moderate acidic conditions Научная публикация

Журнал Mendeleev Communications
ISSN: 0959-9436
Вых. Данные Год: 2018, Том: 28, Номер: 1, Страницы: 27-28 Страниц : 2 DOI: 10.1016/j.mencom.2018.01.007
Авторы Genaev Alexander M. 1 , Salnikov George E. 1,2 , Shernyukov Andrey V. 1 , Zhu Zhongwei 2 , Koltunov Konstantin Yu. 2,3
Организации
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Dept Nat Sci, Novosibirsk 630090, Russia
3 (Данные Web of science) Russian Acad Sci, GK Boreskov Inst Catalysis, Siberian Branch, Novosibirsk 630090, Russia

Реферат: Compared with the parent 1,1'-bi-2-naphthol (BINOL), its dimethyl ether is highly resistant towards racemization under moderate acidic conditions. This finding confirms the hypothetical mechanism of BINOL atropisomerization including internal rotation around the C-sp3(1)-C-sp3(1)' bond in its protonated forms.
Библиографическая ссылка: Genaev A.M. , Salnikov G.E. , Shernyukov A.V. , Zhu Z. , Koltunov K.Y.
Enhanced enantiostability of BINOL dimethyl ether under moderate acidic conditions
Mendeleev Communications. 2018. V.28. N1. P.27-28. DOI: 10.1016/j.mencom.2018.01.007 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 янв. 2018 г.
Идентификаторы БД:
Web of science: WOS:000425204700007
Scopus: 2-s2.0-85041595732
РИНЦ: 35514582
OpenAlex: W2792904275
Цитирование в БД:
БД Цитирований
Web of science 4
Scopus 4
РИНЦ 5
OpenAlex 5
Альметрики: