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Plant coumarins: XI. Cross coupling reactions with 2-(tosyl)oreoselone Научная публикация

Журнал Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Вых. Данные Год: 2013, Том: 49, Номер: 1, Страницы: 99-107 Страниц : 9 DOI: 10.1134/S107042801301017X
Авторы Lipeeva A.B. 1 , Shul'ts E.E. 1 , Shakirov M.M. 1 , Tolstikov G.A. 1
Организации
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Реферат: The reaction of a linearly fused furocoumarin, oreoselone, with p-toluenesulfonyl chloride gave 2-tosyloreoselone which showed a high reactivity in palladium-catalyzed cross-coupling reactions with formation of a new carbon-carbon bond. 2-Tosyloreoselone reacted with terminal alkynes in the presence of Pd(PPh3)(2)Cl-2 to give the corresponding 2-alkynylfuro[3,2-g]chromen-3-ones. 2-Aryl(hetaryl)alkynyloreoselones were obtained in high yield directly by palladium-catalyzed reaction of oreoselone with tosyl chloride and aryl(hetaryl)acetylenes. The reaction of 2-tosyloreoselone with aryl(hetaryl)boronic acids in the presence of palladium complexes with uni- and bidentate ligands, tetrabutylammonium bromide, and a base afforded 2-aryl(hetaryl)-substituted oreoselones. 2-Vinyloreoselone was synthesized from 2-tosyloreoselone and potassium trifluoro(vinyl)borate. DOI: 10.1134/S107042801301017X
Библиографическая ссылка: Lipeeva A.B. , Shul'ts E.E. , Shakirov M.M. , Tolstikov G.A.
Plant coumarins: XI. Cross coupling reactions with 2-(tosyl)oreoselone
Russian Journal of Organic Chemistry. 2013. V.49. N1. P.99-107. DOI: 10.1134/S107042801301017X WOS Scopus РИНЦ OpenAlex
Оригинальная: Липеева А.В. , Шульц Э.Э. , Шакиров М.М. , Толстиков Г.А.
Исследование растительных кумаринов xi. реакции кросс-сочетания с участием 2-(тозил)ореозелона
Журнал органической химии (RUSS J ORG CHEM+). 2013. Т.49. №1. С.105-112. РИНЦ
Даты:
Опубликована в печати: 1 янв. 2013 г.
Опубликована online: 8 февр. 2013 г.
Идентификаторы БД:
Web of science: WOS:000314696400017
Scopus: 2-s2.0-84873653584
РИНЦ: 20433258
OpenAlex: W2030050453
Цитирование в БД:
БД Цитирований
Web of science 5
Scopus 5
РИНЦ 4
OpenAlex 4
Альметрики: