Stereoselective synthesis of functionalized perhydropyrrolo[1,2- b ]isoxazoles based on (3 + 2)-annulation of donor–acceptor cyclopropanes and isoxazolines Научная публикация
| Журнал |
Organic and Biomolecular Chemistry
ISSN: 1477-0520 , E-ISSN: 1477-0539 |
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| Вых. Данные | Год: 2026, Том: 24, Номер: 1, Страницы: 207-215 Страниц : 9 DOI: 10.1039/d5ob01604e | ||||||
| Авторы |
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| Организации |
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Информация о финансировании (1)
| 1 | Институт органической химии им. Н. Д. Зелинского Российской академии наук |
Реферат:
A stereoselective route to access substituted pyrrolidine cores via Lewis acid catalyzed (3 + 2)-annulation of donor–acceptor cyclopropanes (DACs) and isoxazolines has been developed. Exclusive cis-2,5-stereoselectivity was governed by kinetically controlled conditions using Sn(OTf)2 as the catalyst, while excellent trans-2,5-stereoselectivity was achieved by thermodynamically controlled conditions using Sc(OTf)3 as the catalyst. For DACs bearing electron-poor substituents, Yb(NTf2)3 proved to be the most efficient catalyst due to its higher Lewis acidity compared to triflates. The isoxazoline (3 + 2)-annulation reaction was also extended to bicyclo[1.1.0]butanes (BCBs), providing easy access to the 2-azabicyclo[2.1.1]hexane core, which may be considered as a promising 3D-bioisosteric replacement for pyrrole and pyrrolidine motifs.
Библиографическая ссылка:
Potapov K.V.
, Novikov M.A.
, Kozmenko Y.V.
, Solyev P.N.
, Volodin A.D.
, Korlyukov A.A.
, Novikov R.A.
, Tomilov Y.V.
Stereoselective synthesis of functionalized perhydropyrrolo[1,2- b ]isoxazoles based on (3 + 2)-annulation of donor–acceptor cyclopropanes and isoxazolines
Organic and Biomolecular Chemistry. 2026. V.24. N1. P.207-215. DOI: 10.1039/d5ob01604e WOS Scopus OpenAlex
Stereoselective synthesis of functionalized perhydropyrrolo[1,2- b ]isoxazoles based on (3 + 2)-annulation of donor–acceptor cyclopropanes and isoxazolines
Organic and Biomolecular Chemistry. 2026. V.24. N1. P.207-215. DOI: 10.1039/d5ob01604e WOS Scopus OpenAlex
Идентификаторы БД:
| Web of science: | WOS:001631382700001 |
| Scopus: | 2-s2.0-105023841662 |
| OpenAlex: | W4416736238 |
Цитирование в БД:
| БД | Цитирований |
|---|---|
| OpenAlex | Нет цитирований |
| Scopus | Нет цитирований |