Extended Corey–Chaykovsky reactions: transformation of 2-hydroxychalcones to benzannulated 2,8-dioxabicyclo[3.2.1]octanes and 2,3-dihydrobenzofurans Научная публикация
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Organic Chemistry Frontiers
ISSN: 2052-4110 , E-ISSN: 2052-4129 |
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| Вых. Данные | Год: 2022, Том: 9, Номер: 3, Страницы: 737-744 Страниц : 8 DOI: 10.1039/d1qo01646f | ||||||||
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Реферат:
We report the divergent synthesis of benzannulated 2,8-dioxabicyclo[3.2.1]octanes and 2,3-dihydrobenzofurans using the concept of extended Corey–Chaykovsky reactions. With this concept, 2-hydroxychalcones were treated with the Corey ylide providing highly reactive donor–acceptor cyclopropanes that were introduced in a one pot manner for further transformations. We demonstrated that the nucleophilic three-membered ring opening followed by cyclization under mild reaction conditions afforded the 2,8-dioxabicyclo[3.2.1]octane scaffold. On the other hand, heating the intermediates with a strong Brønsted acid furnished 2-phenacyl-2,3-dihydrobenzofurans. These transformations, resulting in products with crucially different heterocyclic skeletons from the same starting compounds, demonstrate the enormous potential of the extended Corey–Chaykovsky reaction.
Библиографическая ссылка:
Fadeev A.A.
, Makarov A.S.
, Ivanova O.A.
, Uchuskin M.G.
, Trushkov I.V.
Extended Corey–Chaykovsky reactions: transformation of 2-hydroxychalcones to benzannulated 2,8-dioxabicyclo[3.2.1]octanes and 2,3-dihydrobenzofurans
Organic Chemistry Frontiers. 2022. V.9. N3. P.737-744. DOI: 10.1039/d1qo01646f WOS Scopus OpenAlex
Extended Corey–Chaykovsky reactions: transformation of 2-hydroxychalcones to benzannulated 2,8-dioxabicyclo[3.2.1]octanes and 2,3-dihydrobenzofurans
Organic Chemistry Frontiers. 2022. V.9. N3. P.737-744. DOI: 10.1039/d1qo01646f WOS Scopus OpenAlex
Идентификаторы БД:
| Web of science: | WOS:000732841800001 |
| Scopus: | 2-s2.0-85124553412 |
| OpenAlex: | W4200460627 |