Conformational Lability of Bispidine as a Route to New Polycyclic Compounds Научная публикация
| Журнал |
Journal of Organic Chemistry
ISSN: 1520-6904 , E-ISSN: 0022-3263 |
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| Вых. Данные | Год: 2026, Том: 91, Номер: 43, Страницы: 14341–14345 Страниц : DOI: 10.1021/acs.joc.6c01744 | ||
| Авторы |
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| Организации |
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Реферат:
In this study, novel tricyclic compounds based on bispidine were prepared via a Michael addition−Henry domino reaction.
This reaction sequence proceeds under mild conditions with high diastereoselectivity. Postsynthetic transformation pathways for
the resulting nitro alcohols were demonstrated, leading to tricyclic amino alcohols of various structures.
Библиографическая ссылка:
Medved'ko A.V.
, Vatsadze S.Z.
Conformational Lability of Bispidine as a Route to New Polycyclic Compounds
Journal of Organic Chemistry. 2026. V.91. N43. P.14341–14345. DOI: 10.1021/acs.joc.6c01744 WOS Scopus OpenAlex
Conformational Lability of Bispidine as a Route to New Polycyclic Compounds
Journal of Organic Chemistry. 2026. V.91. N43. P.14341–14345. DOI: 10.1021/acs.joc.6c01744 WOS Scopus OpenAlex
Даты:
| Поступила в редакцию: | 20 июл. 2026 г. |
| Принята к публикации: | 13 окт. 2026 г. |
| Опубликована в печати: | 20 окт. 2026 г. |
| Опубликована online: | 30 окт. 2026 г. |
Идентификаторы БД:
| ≡ Web of science: | WOS:001907901000001 |
| ≡ Scopus: | 2-s2.0-105055012290 |
| ≡ OpenAlex: | W7223064614 |