Ionic Hydrogenation of 1-Naphthol Derivatives with Alkanes in the Presence of Aluminum Halides | Sciact - CRIS-система Института катализа

Ionic Hydrogenation of 1-Naphthol Derivatives with Alkanes in the Presence of Aluminum Halides Научная публикация

Журнал

Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393

Вых. Данные

Год: 1997, Том: 33, Номер: 5, Страницы: 689-693 Страниц : 5

Авторы

Koltunov K.Y. ¹ , Subbotina E.N. ¹ , Repinskaya I.B. ¹

Организации

1	Novosibirsk Inst. of Organ. Chem., Siberian Division, Russian Academy of Sciences, pr. Akademika Lavrent'eva 9, Novosibirsk, 630090, Russian Federation

Reactions of 1-naphthol, 4-methyl-1-naphthol, 3-phenyl-1-naphthol, and 4-chloro-1-naphthol with cyclohexane, as well as of 1-naphthol with methylcyclopentane, pentane, isobutane, and propane, in the presence of excess aluminum chloride or bromide yield α-tetralone derivatives as a result of regioselective ionic hydrogenation. Abstraction of the hydride ion from alkane is effected by the protonated complex of the keto form of the naphthol with aluminum halide.

Koltunov K.Y. , Subbotina E.N. , Repinskaya I.B.
Ionic Hydrogenation of 1-Naphthol Derivatives with Alkanes in the Presence of Aluminum Halides
Russian Journal of Organic Chemistry. 1997. V.33. N5. P.689-693. Scopus РИНЦ CAPlusCA

Колтунов К.Ю. , Субботина Е.Н. , Репинская Т.Б.
Ионное гидрирование производных 1-нафтола алканами в присутствии галогенидов алюминия
Журнал органической химии. 1997. Т.33. №5. С.750-754.

Опубликована в печати:

1 мая 1997 г.

Scopus:	2-s2.0-0031323465
РИНЦ:	13259356
Chemical Abstracts:	1998:169150
Chemical Abstracts (print):	128:230114

БД	Цитирований
Scopus	22