Preparation of peri-annulated indoles from polynitro compounds Научная публикация
| Журнал |
Tetrahedron
ISSN: 0040-4020 , E-ISSN: 1464-5416 |
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| Вых. Данные | Год: 2009, Том: 65, Номер: 34, Страницы: 6868-6872 Страниц : 5 DOI: 10.1016/j.tet.2009.06.074 | ||
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| Организации |
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Реферат:
A novel peri-annulated heterocyclic system of 1,2-dihydrobenz[6,7]oxepino[4,3,2-cd]indole was prepared starting from TNT via 4,6-dinitro-1-tosylindoline as a key intermediate. Base-induced Cdouble bondC bond shift in 1,2-dihydrobenz[6,7]oxepino[4,3,2-cd]indoles affords isomeric 2,11-dihydrobenz[6,7]oxepino[4,3,2-cd]indoles.
Библиографическая ссылка:
Samet A.V.
, Yamskov A.N.
, Strelenko Y.A.
, Semenov V.V.
Preparation of peri-annulated indoles from polynitro compounds
Tetrahedron. 2009. V.65. N34. P.6868-6872. DOI: 10.1016/j.tet.2009.06.074 WOS Scopus OpenAlex
Preparation of peri-annulated indoles from polynitro compounds
Tetrahedron. 2009. V.65. N34. P.6868-6872. DOI: 10.1016/j.tet.2009.06.074 WOS Scopus OpenAlex
Идентификаторы БД:
| Web of science: | WOS:000269282400014 |
| Scopus: | 2-s2.0-67650717992 |
| OpenAlex: | W2949692394 |