Oxidative alkylamination of 1,5-dihydroxynaphthalenes. Synthesis and tautomeric transformations of N-alkyl-5-hydroxy-1,4-naphthoquinone 4-imines Научная публикация
| Журнал |
Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393 |
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| Вых. Данные | Год: 2000, Том: 36, Номер: 9, Страницы: 1312-1315 Страниц : 4 | ||
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Реферат:
Oxidation of 1,5-dihydroxy-, 2,6-dibromo-1,5-dihydroxy-, and 2,4,6,8-tetrabromo-1,5-dihydroxy-naphthalenes with Ag2O or PbO2 in the presence of butylamine or methylamine leads to formation of the corresponding 4-alkylamino-and 2,4-bis(alkylamino)-1,5-naphthoquinone which exist in organic solvents as tautomeric mixtures with N-alkyl-5-hydroxy-1,4-naphthoquinone 4-imines.
Библиографическая ссылка:
Bukhtoyarova A.D.
, Ektova L.V.
Oxidative alkylamination of 1,5-dihydroxynaphthalenes. Synthesis and tautomeric transformations of N-alkyl-5-hydroxy-1,4-naphthoquinone 4-imines
Russian Journal of Organic Chemistry. 2000. V.36. N9. P.1312-1315. WOS Scopus РИНЦ
Oxidative alkylamination of 1,5-dihydroxynaphthalenes. Synthesis and tautomeric transformations of N-alkyl-5-hydroxy-1,4-naphthoquinone 4-imines
Russian Journal of Organic Chemistry. 2000. V.36. N9. P.1312-1315. WOS Scopus РИНЦ
Идентификаторы БД:
| Web of science: | WOS:000168014200011 |
| Scopus: | 2-s2.0-0034257777 |
| РИНЦ: | 13345412 |