Reaction of 6-nitro-2, 9-dioxa-1-azabicyclo[4.3.0]nonane derivatives with nucleophiles Научная публикация
| Журнал |
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science
ISSN: 2376-8444 , E-ISSN: 0568-5230 |
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| Вых. Данные | Год: 1978, Том: 27, Номер: 11, Страницы: 2371-2373 Страниц : 3 DOI: 10.1007/bf00946705 | ||
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Реферат:
1. In 6-nitro-2,9-dioxa-1-azabicyclo[4.3.0]nonane derivatives when reacted with sodium azide in aqueous acetone the nitro group is replaced by the azido group. 2. The reaction of 6-nitro-8-phenyl-2, 9-dioxa-1-azabicyclo[4.3.0]nonane with diethylamine in abs. THF, or with the K salt of nitroethane in aqueous DMF, leads to replacement of the nitro group by hydroxyl. 3. 3-(γ-Hydroxypropyl)-5-phenylisoxazoline is formed when 6-nitro-8-phenyl-2,9-dioxa-1-azabicyclo[4.3.0]nonane is reacted with NaHS.
Библиографическая ссылка:
Chlenov I.E.
, Pal'tseva G.D.
, Petrova I.M.
, Shitkin V.M.
, Tartakovskii V.A.
Reaction of 6-nitro-2, 9-dioxa-1-azabicyclo[4.3.0]nonane derivatives with nucleophiles
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science. 1978. V.27. N11. P.2371-2373. DOI: 10.1007/bf00946705 OpenAlex
Reaction of 6-nitro-2, 9-dioxa-1-azabicyclo[4.3.0]nonane derivatives with nucleophiles
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science. 1978. V.27. N11. P.2371-2373. DOI: 10.1007/bf00946705 OpenAlex
Идентификаторы БД:
| OpenAlex: | W2953046784 |
Цитирование в БД:
| БД | Цитирований |
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| OpenAlex | 1 |