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GaCl3-promoted C–H functionalization of ethylidenemalonate in reactions with internal alkynes Научная публикация

Журнал Organic & Biomolecular Chemistry
ISSN: 1477-0520 , E-ISSN: 1477-0539
Вых. Данные Год: 2026, DOI: 10.1039/d6ob00875e
Авторы Borisov Denis D. 1 , Borisova Irina A. 1 , Antanyazov Mikhail R. 1,2 , Prolomov Ilya V. 1 , Medvedev Michael G. 1 , Novikov Roman A. 1 , Tomilov Yury V. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991 Moscow, Russian Federation
2 Lomonosov Moscow State University, Leninskie Gory 1/3, 119991 Moscow, Russian Federation

Реферат: The unprecedented C(sp2)–H functionalization of ethylidenemalonate with internal alkynes was discovered, leading to substituted vinylcyclopentanes as trans,trans-isomers (dr > 15 : 1). The experiment with deuterated ethylidenemalonate showed that the formation of substituted vinylcyclopentane is accompanied by a 1,2-hydride shift and mono-γ-C–H insertion into the internal alkyne.
Библиографическая ссылка: Borisov D.D. , Borisova I.A. , Antanyazov M.R. , Prolomov I.V. , Medvedev M.G. , Novikov R.A. , Tomilov Y.V.
GaCl3-promoted C–H functionalization of ethylidenemalonate in reactions with internal alkynes
Organic & Biomolecular Chemistry. 2026. DOI: 10.1039/d6ob00875e WOS Scopus OpenAlex
Даты:
Поступила в редакцию: 5 июн. 2026 г.
Принята к публикации: 31 июл. 2026 г.
Опубликована online: 4 сент. 2026 г.
Идентификаторы БД:
≡ Web of science: WOS:001869655800001
≡ Scopus: 2-s2.0-105049675621
≡ OpenAlex: W7208766654
Альметрики: