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 |
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Output data | Year: 1997, Volume: 33, Number: 5, Pages: 689-693 Pages count : 5 | ||
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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
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.
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 |
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Scopus | 22 |