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Reaction of guaianolide achillin with chlorine in methanol Full article

Journal Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Output data Year: 2000, Volume: 49, Number: 9, Pages: 1624-1628 Pages count : DOI: 10.1007/BF02495170
Tags sesquiterpenoids; guaianolides; achillin; chlorination; two-dimensional NMR spectroscopy; X-ray diffraction analysis
Authors Alebastrov OV , Raldugin VA , Shakirov MM , Bagryanskaya IY , Gatilov YV , Kulyjasov AT , Adekenov SM , Tolstikov GA
Affiliations
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

Abstract: 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.
Cite: 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
Dates:
Published print: Sep 1, 2000
Identifiers:
≡ Web of science: WOS:000171958400024
≡ Scopus: 2-s2.0-0034258426
≡ Elibrary: 13345432
≡ OpenAlex: W2950618679
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