Reductive Deletion of Endocyclic Oxygen Atom in 1,2‐Oxazine N ‐Oxides to Access N ‐Hydroxypyrrolidines Научная публикация
| Журнал |
European Journal of Organic Chemistry
ISSN: 1434-193X , E-ISSN: 1099-0690 |
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| Вых. Данные | Год: 2026, Номер статьи : e70863, Страниц : DOI: 10.1002/ejoc.70863 | ||||||
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Реферат:
Single‐atom ring‐editing strategies have emerged as a powerful tool for the diversification of molecular libraries through the
remodeling of key heterocyclic scaffolds. The 1,2‐oxazine core represents an ideal platform for implementing single heteroatom
deletion/swapping strategies, which lead to five‐membered O‐ or N‐heterocycles with varying levels of saturation. Here, we
introduce a novel reductive ring contraction of 1,2‐oxazine N‐oxides that achieves the formal deletion of the endocyclic oxygen
atom, delivering synthetically valuable N‐hydroxypyrrolidines. This process operates under mild reductive conditions with the
NaBH3CN/TsOH system via an unprecedented multistep ring opening/ring reconstruction sequence. The introduction of a
recyclable chiral auxiliary enables a practical asymmetric variant, providing a route to enantioenriched N‐hydroxypyrrolidines.
Библиографическая ссылка:
Pospelov E.V.
, Zharov N.P.
, Sukhorukov A.Y.
Reductive Deletion of Endocyclic Oxygen Atom in 1,2‐Oxazine N ‐Oxides to Access N ‐Hydroxypyrrolidines
European Journal of Organic Chemistry. 2026. e70863 . DOI: 10.1002/ejoc.70863 WOS Scopus OpenAlex
Reductive Deletion of Endocyclic Oxygen Atom in 1,2‐Oxazine N ‐Oxides to Access N ‐Hydroxypyrrolidines
European Journal of Organic Chemistry. 2026. e70863 . DOI: 10.1002/ejoc.70863 WOS Scopus OpenAlex
Даты:
| Поступила в редакцию: | 23 июл. 2026 г. |
| Принята к публикации: | 11 сент. 2026 г. |
| Опубликована online: | 26 сент. 2026 г. |
Идентификаторы БД:
| ≡ Web of science: | WOS:001885308400001 |
| ≡ Scopus: | 2-s2.0-105051526583 |
| ≡ OpenAlex: | W7214475943 |