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Ionic Hydrogenation of 1-Naphthol Derivatives with Alkanes in the Presence of Aluminum Halides Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 1997, Volume: 33, Number: 5, Pages: 689-693 Pages count : 5
Authors Koltunov K.Y. 1 , Subbotina E.N. 1 , Repinskaya I.B. 1
Affiliations
1 Novosibirsk Inst. of Organ. Chem., Siberian Division, Russian Academy of Sciences, pr. Akademika Lavrent'eva 9, Novosibirsk, 630090, Russian Federation

Abstract: 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.
Cite: 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 ANCAN
Original: 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.
Dates:
Published print: May 1, 1997
Identifiers:
Scopus: 2-s2.0-0031323465
Elibrary: 13259356
Chemical Abstracts: 1998:169150
Chemical Abstracts (print): 128:230114
Citing:
DB Citing
Scopus 22