Reaction of guaianolide achillin with chlorine in methanol Full article
| Journal |
Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171 |
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| 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 |
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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
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 |