Synthesis of 1,2-Diazepines by the Bischler–Napieralski Reaction
- Авторы: Muratov A.V.1, Grebenyuk S.A.1, Eresko A.B.1
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Учреждения:
- Litvinenko Institute of Physical Organic and Coal Chemistry
- Выпуск: Том 54, № 6 (2018)
- Страницы: 861-866
- Раздел: Article
- URL: https://bakhtiniada.ru/1070-4280/article/view/218056
- DOI: https://doi.org/10.1134/S1070428018060064
- ID: 218056
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Аннотация
A new strategy has been proposed for the synthesis of 5H-[1]benzofuro[2,3-d][1,2]diazepines containing two aryl substituents in the diazepine fragment. The key stage of the synthesis is intramolecular cyclization of the corresponding hydrazides under the Bischler–Napieralski reaction conditions.
Об авторах
A. Muratov
Litvinenko Institute of Physical Organic and Coal Chemistry
Email: a_eresko77@mail.ru
Украина, ul. R. Lyuksemburg 70, Donetsk, 83114
S. Grebenyuk
Litvinenko Institute of Physical Organic and Coal Chemistry
Email: a_eresko77@mail.ru
Украина, ul. R. Lyuksemburg 70, Donetsk, 83114
A. Eresko
Litvinenko Institute of Physical Organic and Coal Chemistry
Автор, ответственный за переписку.
Email: a_eresko77@mail.ru
Украина, ul. R. Lyuksemburg 70, Donetsk, 83114
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