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Regio- and diastereoselective access to densely functionalized ketones via the Boekelheide rearrangement of isoxazoline N-oxides Научная публикация

Журнал Organic & Biomolecular Chemistry
ISSN: 1477-0520 , E-ISSN: 1477-0539
Вых. Данные Год: 2022, Том: 20, Номер: 28, Страницы: 5624-5637 Страниц : 14 DOI: 10.1039/d2ob00787h
Авторы Ushakov Pavel Yu. 1 , Ioffe Sema L. 1 , Sukhorukov Alexey Yu. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, 119991, Leninsky prospect, 47, Moscow, Russian Federation

Реферат: In this work, the classical “isoxazoline route” toward aldols involving the [3 + 2]-cycloaddition of nitrile oxide to alkenes and hydrogenolysis of the oxime group was revisited. To avoid regioselectivity issues, [4 + 1]-annulation of nitroalkenes with sulfonium ylides was used to construct the isoxazoline ring bearing an N-oxide moiety. Subsequent deoxygenative C–H functionalization using the Boekelheide rearrangement and hydrogenolysis of the isoxazoline ring afforded α′-acyloxy-substituted aldols, which are difficult to access both by the classical aldol reaction and the “isoxazoline route”. The products are formed in good to high overall yields and as single diastereomers in most cases. The synthetic use of these aldols was showcased by their smooth transformation into diastereomerically pure triols and a 2,3-diaryl-4-hydroxy-substituted tetrahydrofuran derivative, which is structurally related to cinncassin B.
Библиографическая ссылка: Ushakov P.Y. , Ioffe S.L. , Sukhorukov A.Y.
Regio- and diastereoselective access to densely functionalized ketones via the Boekelheide rearrangement of isoxazoline N-oxides
Organic & Biomolecular Chemistry. 2022. V.20. N28. P.5624-5637. DOI: 10.1039/d2ob00787h WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000821585600001
Scopus: 2-s2.0-85133976095
OpenAlex: W4284881388
Цитирование в БД:
БД Цитирований
OpenAlex 9
Scopus 9
Web of science 9
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