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Reaction of guaianolide achillin with chlorine in methanol Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Вых. Данные Год: 2000, Том: 49, Номер: 9, Страницы: 1624-1628 Страниц : DOI: 10.1007/BF02495170
Ключевые слова sesquiterpenoids; guaianolides; achillin; chlorination; two-dimensional NMR spectroscopy; X-ray diffraction analysis
Авторы Alebastrov OV , Raldugin VA , Shakirov MM , Bagryanskaya IY , Gatilov YV , Kulyjasov AT , Adekenov SM , Tolstikov GA
Организации
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia
2 (Данные Web of science) Minist Sci & Higher Educ Kazakhstan Republ, Inst Phytochem, Karaganda 470032, Kazakhstan

Реферат: The reaction of sesquiterpene lactone achillin with chlorine in methanol afforded four products, viz., two monochlorides and two dichlorides. One of these monochlorides is an intermediate in the formation of both dichlorides. The structures of the reaction products were established by two-dimensional NMR spectroscopy. The structure of one of the products was also established by X-ray diffraction analysis.
Библиографическая ссылка: Alebastrov O. , Raldugin V. , Shakirov M. , Bagryanskaya I. , Gatilov Y. , Kulyjasov A. , Adekenov S. , Tolstikov G.
Reaction of guaianolide achillin with chlorine in methanol
Russian Chemical Bulletin. 2000. V.49. N9. P.1624-1628. DOI: 10.1007/BF02495170 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 сент. 2000 г.
Идентификаторы БД:
≡ Web of science: WOS:000171958400024
≡ Scopus: 2-s2.0-0034258426
≡ РИНЦ: 13345432
≡ OpenAlex: W2950618679
Альметрики: