GaCl3‐Promoted Reactions of Donor‐Acceptor Cyclopropanes with Conjugated Diacetylenes Научная публикация
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Asian Journal of Organic Chemistry
ISSN: 2193-5815 , E-ISSN: 2193-5807 |
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| Вых. Данные | Год: 2025, Том: 14, Номер: 9, Страницы: e00392 Страниц : DOI: 10.1002/ajoc.202500392 | ||||
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Реферат:
The reaction of 1,2-zwitterionic complexes of 2-arylcyclopropane-1,1-dicarboxylates (ACDC), generated using gallium trichloride, with conjugated substituted diacetylenes was studied. The series of the substituted 1,1′-binaphthalenes were obtained in yields up to 57%. The reaction occurs via a cascade addition/annulation/elimination pathway involving both triple bonds of conjugated diacetylenes. The regioselectivity of this process was studied, and it was shown that binaphthalenes formed exclusively as 1,1′-regioisomers.
Библиографическая ссылка:
Borisova I.A.
, Borisov D.D.
, Kolotyrkina N.G.
, Zhou B.
, Ye L.
, Novikov R.A.
, Tomilov Y.V.
GaCl3‐Promoted Reactions of Donor‐Acceptor Cyclopropanes with Conjugated Diacetylenes
Asian Journal of Organic Chemistry. 2025. V.14. N9. P.e00392. DOI: 10.1002/ajoc.202500392 WOS Scopus OpenAlex
GaCl3‐Promoted Reactions of Donor‐Acceptor Cyclopropanes with Conjugated Diacetylenes
Asian Journal of Organic Chemistry. 2025. V.14. N9. P.e00392. DOI: 10.1002/ajoc.202500392 WOS Scopus OpenAlex
Идентификаторы БД:
| ≡ Web of science: | WOS:001532796900001 |
| ≡ Scopus: | 2-s2.0-105011250588 |
| ≡ OpenAlex: | W4412567504 |