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Facile Synthesis of Natural Alkoxynaphthalene Analogues from Plant Alkoxybenzenes Научная публикация

Журнал Journal of Natural Products
ISSN: 0163-3864 , E-ISSN: 1520-6025
Вых. Данные Год: 2016, Том: 79, Номер: 4, Страницы: 923-928 Страниц : 6 DOI: 10.1021/acs.jnatprod.5b01007
Авторы Tsyganov Dmitry V. 1 , Krayushkin Mikhail M. 1 , Konyushkin Leonid D. 1 , Strelenko Yuri A. 1 , Semenova Marina N. 2,3 , Semenov Victor V. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, RAS, Leninsky Prospect, 47, 119991, Moscow, Russian Federation
2 Chemical Block Ltd., 3 Kyriacou Matsi, 3723, Limassol, Cyprus
3 Institute of Developmental Biology, RAS, Vavilov Street, 26, 119334, Moscow, Russian Federation

Реферат: Analogues of the bioactive natural alkoxynaphthalene pycnanthulignene D were synthesized by an efficient method. The starting plant allylalkoxybenzenes (1) are easily available from the plant essential oils of sassafras, dill, and parsley. The target 1-arylalkoxynaphthalenes (5) exhibited antiproliferative activity in a phenotypic sea urchin embryo assay.
Библиографическая ссылка: Tsyganov D.V. , Krayushkin M.M. , Konyushkin L.D. , Strelenko Y.A. , Semenova M.N. , Semenov V.V.
Facile Synthesis of Natural Alkoxynaphthalene Analogues from Plant Alkoxybenzenes
Journal of Natural Products. 2016. V.79. N4. P.923-928. DOI: 10.1021/acs.jnatprod.5b01007 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000374915800033
Scopus: 2-s2.0-84967317320
OpenAlex: W2281096563
Цитирование в БД:
БД Цитирований
OpenAlex 6
Scopus 7
Web of science 7
Альметрики: