A novel method for the sterically shielded pyrrolidine nitroxides synthesis using donor–acceptor cyclopropanes Научная публикация
Журнал |
Tetrahedron Letters
ISSN: 0040-4039 |
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Вых. Данные | Год: 2023, Том: 123, Страницы: 154546 Страниц : 1 DOI: 10.1016/j.tetlet.2023.154546 | ||||
Авторы |
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Организации |
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Информация о финансировании (1)
1 | Российский Научный Фонд | 21-73-00281 |
Реферат:
Sterically shielded nitroxides were shown to demonstrate resistance to bioreduction. For this reason, they are attracting much interest as spin labels and probes for in-cell and in vivo EPR and NMR applications. Formal [3 + 2] cycloaddition reaction of donor–acceptor cyclopropanes with propionitrile provided 1-pyrrolines which were converted to the new sterically shielded achiral pyrrolidine nitroxides via several steps.
Библиографическая ссылка:
Taratayko A.I.
, Trakhinina S.Y.
, Lomanovich K.A.
, Kirilyuk I.A.
A novel method for the sterically shielded pyrrolidine nitroxides synthesis using donor–acceptor cyclopropanes
Tetrahedron Letters. 2023. V.123. P.154546. DOI: 10.1016/j.tetlet.2023.154546 WOS РИНЦ
A novel method for the sterically shielded pyrrolidine nitroxides synthesis using donor–acceptor cyclopropanes
Tetrahedron Letters. 2023. V.123. P.154546. DOI: 10.1016/j.tetlet.2023.154546 WOS РИНЦ
Даты:
Поступила в редакцию: | 10 апр. 2023 г. |
Принята к публикации: | 8 мая 2023 г. |
Опубликована online: | 12 мая 2023 г. |
Идентификаторы:
Web of science | WOS:001012380900001 |
РИНЦ | 61808483 |
OpenAlex | W4376126308 |