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An Intramolecular Nitroso-Meerwein–Ponndorf–Verley–Oppenauer Reaction to Access Fused Pyrrolidine Scaffolds Научная публикация

Журнал Organic Letters
ISSN: 1523-7060 , E-ISSN: 1523-7052
Вых. Данные Год: 2024, Том: 26, Номер: 2, Страницы: 450-455 Страниц : 6 DOI: 10.1021/acs.orglett.3c03552
Авторы Malykhin Roman S. 1 , Aksenova Svetlana A. 2,3 , Sukhorukov Alexey Yu. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prospect 47, Moscow 119991, Russian Federation
2 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Vavilova str. 28, Moscow 119991, Russian Federation
3 Moscow Institute of Physics and Technology (National Research University), Institutskiy per. 9, Dolgoprudny 141700, Moscow Region, Russian Federation

Реферат: δ-Hydroxy chloronitroso compounds generated in situ from 1,2-oxazine N-oxides undergo a 1,5-hydride transfer related to the Meerwein–Ponndorf–Verley–Oppenauer reaction. Based on the process discovered, a three-step access to fused pyrrolidine scaffolds containing up to four contiguous stereogenic centers starting from simple nitrostyrenes and cycloalkenes or cyclodienes has been developed. The suggested reaction mechanism was confirmed by in situ UV–vis and ATR FT-IR monitoring and DFT calculations.
Библиографическая ссылка: Malykhin R.S. , Aksenova S.A. , Sukhorukov A.Y.
An Intramolecular Nitroso-Meerwein–Ponndorf–Verley–Oppenauer Reaction to Access Fused Pyrrolidine Scaffolds
Organic Letters. 2024. V.26. N2. P.450-455. DOI: 10.1021/acs.orglett.3c03552 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:001146483300001
Scopus: 2-s2.0-85182578463
OpenAlex: W4390660954
Цитирование в БД:
БД Цитирований
OpenAlex 6
Scopus 6
Web of science 6
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