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Polyalkoxy-substituted nitrostilbenes in the synthesis of lamellarin analogs. Formal synthesis of lamellarin H Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Вых. Данные Год: 2023, Том: 72, Номер: 9, Страницы: 2090-2094 Страниц : 5 DOI: 10.1007/s11172-023-4003-y
Авторы Silyanova E.A. 1 , Maksimenko A.S. 1 , Brunner M.D. 1 , Koblov I.A. 1 , Kislyi V.P. 1 , Samet A.V. 1 , Semenov V.V. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Реферат: Lamellarin D trimethyl ether was prepared by 1,3-dipolar cycloaddition of 6,7-dimethoxyisoquinolinium ylide to pentamethoxy-substituted nitrostilbene followed by a lactone ring closure in the intermediate cycloadduct. This approach allowed a formal synthesis of lamellarin H.
Библиографическая ссылка: Silyanova E.A. , Maksimenko A.S. , Brunner M.D. , Koblov I.A. , Kislyi V.P. , Samet A.V. , Semenov V.V.
Polyalkoxy-substituted nitrostilbenes in the synthesis of lamellarin analogs. Formal synthesis of lamellarin H
Russian Chemical Bulletin. 2023. V.72. N9. P.2090-2094. DOI: 10.1007/s11172-023-4003-y WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:001074328300014
Scopus: 2-s2.0-85172144715
OpenAlex: W4387053675
Цитирование в БД:
БД Цитирований
OpenAlex 6
Scopus 5
Web of science 6
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