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SYNTHESIS OF HYBRID MOLECULES CONTAINING FRAGMENTS OF SESQUITERPENE LACTONES AND PLANT ALKALOIDS Научная публикация

Журнал Chemistry of Natural Compounds
ISSN: 0009-3130 , E-ISSN: 1573-8388
Вых. Данные Год: 2011, Том: 46, Номер: 6, Страницы: 880-885 Страниц : DOI: 10.1007/s10600-011-9774-y
Ключевые слова isoalantolactone; 5'-iodolappaconitine; 6-bromodeoxyvasicinone; Pd acetate; cross-coupling reaction
Авторы Belovodskii A. V. 1 , Shul'ts E. E. 1 , Shakirov M. M. 1 , Romanov V. E. 1 , Elmuradov B. Zh. 2 , Shakhidoyatov Kh. M. 2 , Tolstikov G. A. 1
Организации
1 (Данные Web of science) Russian Acad Sci, NN Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia
2 (Данные Web of science) Acad Sci Uzbek, S Yu Yunusov Inst Chem Plant Subst, Tashkent, Uzbekistan

Реферат: The Pd-catalyzed arylation of isoalantolactone by deoxyvasicinone and lappaconitine halides occurred with formation mainly of cross-coupling products with the (E)-configuration of the double bond. Another three compounds were isolated from the reaction of isoalantolactone with 6-bromodeoxyvasicinone. These were the lactone diarylation product, a compound with the (Z)-configuration of the double bond, and a product with a shift of the C(11,13) double bond and configuration inversion at C(8). The new compounds are interesting as potential biologically active agents.
Библиографическая ссылка: Belovodskii A.V. , Shul'ts E.E. , Shakirov M.M. , Romanov V.E. , Elmuradov B.Z. , Shakhidoyatov K.M. , Tolstikov G.A.
SYNTHESIS OF HYBRID MOLECULES CONTAINING FRAGMENTS OF SESQUITERPENE LACTONES AND PLANT ALKALOIDS
Chemistry of Natural Compounds. 2011. V.46. N6. P.880-885. DOI: 10.1007/s10600-011-9774-y WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 янв. 2011 г.
Опубликована online: 8 февр. 2011 г.
Идентификаторы БД:
Web of science: WOS:000288438500011
Scopus: 2-s2.0-79952696502
РИНЦ: 24939318
OpenAlex: W2009522262
Цитирование в БД:
БД Цитирований
Web of science 14
Scopus 8
РИНЦ 9
OpenAlex 6
Альметрики: