Formation of the pyrroline N-oxide ring by interaction of α-isonitrosoketones-derivatives of tetrahydrobenzofurazan and -furoxan with aldehydes and morpholine and some of the reactions of these compounds Научная публикация
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Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353 |
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| Вых. Данные | Год: 2004, Том: 40, Номер: 10, Страницы: 1346-1351 Страниц : | ||
| Ключевые слова | 4,5,6,7-tetrahydrobenzofurazans; 4,5,6,7-tetrahydrobenzofuroxans; Cinnolines; Enamines; Indolines; Pyrroline N-oxides; α-isonitroso ketones | ||
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Реферат:
α-Isonitroso ketones, derivatives of tetrahydrobenzofurazan and furoxan, react with aldehydes (acetaldehyde and propionaldehyde) and morpholine to form derivatives of tetrahydropyrrolo[2,3-e]-2,1,3-benzoxadiazole 6-oxide. Treatment of the latter with hydrazine hydrate gave derivatives of 4,5-dihydro-1,2,5-oxadiazolo[3,4-f]cinnoline which are readily dehydrogenated with tetrachloro-benzoquinone to derivatives of 1,2,5-oxadiazolo[3,4-f] cinnoline. Reduction of tetrahydropyrrolo[2,3-e]-2,1,3-benzoxadiazole 6-oxides with sodium borohydride gave derivatives of N-hydroxyhexahydro-pyrrolo[2,3-e]-2, 1,3-benzoxazole. © 2004 Springer Science+Business Media, Inc.
Библиографическая ссылка:
Samsonov V.A.
Formation of the pyrroline N-oxide ring by interaction of α-isonitrosoketones-derivatives of tetrahydrobenzofurazan and -furoxan with aldehydes and morpholine and some of the reactions of these compounds
Chemistry of Heterocyclic Compounds. 2004. V.40. N10. P.1346-1351. Scopus РИНЦ
Formation of the pyrroline N-oxide ring by interaction of α-isonitrosoketones-derivatives of tetrahydrobenzofurazan and -furoxan with aldehydes and morpholine and some of the reactions of these compounds
Chemistry of Heterocyclic Compounds. 2004. V.40. N10. P.1346-1351. Scopus РИНЦ
Идентификаторы:
| Scopus | 2-s2.0-14944375363 |
| РИНЦ | 13466878 |