Converting Strain Release into Aromaticity Loss for Activation of Donor–Acceptor Cyclopropanes: Generation of Quinone Methide Traps for C-Nucleophiles Научная публикация
| Журнал |
Organic Letters
ISSN: 1523-7060 , E-ISSN: 1523-7052 |
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| Вых. Данные | Год: 2024, Том: 26, Номер: 38, Страницы: 8177-8182 Страниц : 6 DOI: 10.1021/acs.orglett.4c03106 | ||||||||||
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Реферат:
Here, we present a new approach for the activation of donor–acceptor cyclopropanes in ring-opening reactions, which does not require the use of a Lewis or Brønsted acid as a catalyst. Donor–acceptor cyclopropanes containing a phenolic group as the donor undergo deprotonation and isomerization to form the corresponding quinone methides. This innovative strategy was applied to achieve (4 + 1)-annulation of cyclopropanes with sulfur ylides, affording functionalized dihydrobenzofurans. Additionally, the generated ortho- and para-(aza)quinone methides can be trapped by various CH-acids.
Библиографическая ссылка:
Shorokhov V.V.
, Chabuka B.K.
, Tikhonov T.P.
, Filippova A.V.
, Zhokhov S.S.
, Tafeenko V.A.
, Andreev I.A.
, Ratmanova N.K.
, Uchuskin M.G.
, Trushkov I.V.
, Alabugin I.V.
, Ivanova O.A.
Converting Strain Release into Aromaticity Loss for Activation of Donor–Acceptor Cyclopropanes: Generation of Quinone Methide Traps for C-Nucleophiles
Organic Letters. 2024. V.26. N38. P.8177-8182. DOI: 10.1021/acs.orglett.4c03106 WOS Scopus OpenAlex
Converting Strain Release into Aromaticity Loss for Activation of Donor–Acceptor Cyclopropanes: Generation of Quinone Methide Traps for C-Nucleophiles
Organic Letters. 2024. V.26. N38. P.8177-8182. DOI: 10.1021/acs.orglett.4c03106 WOS Scopus OpenAlex
Идентификаторы БД:
| Web of science: | WOS:001310753000001 |
| Scopus: | 2-s2.0-85203819226 |
| OpenAlex: | W4402472434 |