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Plant coumarins: XIII. Synthesis of 2,3,9-trisubstituted furocoumarins Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 2013, Volume: 49, Number: 3, Pages: 403-411 Pages count : 9 DOI: 10.1134/S1070428013030159
Authors Lipeeva A.V. 1 , Shul'ts E.E. 1 , Shakirov M.M. 1 , Bagryanskaya I.Yu. 1 , Tolstikov G.A. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Abstract: Peucedanin reacted with methylideneiminium salt generated in situ from N,N,N',N'-tetramethylmethanediamine and acetyl chloride to give 2-(dimethylaminomethyl)oreoselone. Reactions of peucedanin with aminomethylating agents generated in situ from formaldehyde and dimethylamine, N-methylpiperazine, or N-Boc-piperazine in boiling methanol smoothly afforded the corresponding 9-aminomethyl derivatives whose hydrolysis produced 9-aminomethyl-substituted oreoselones. 2,3,9-Trisubstituted linearly fused furocoumarins were synthesized by reactions of 9-substituted oreoselone trifluoromethanesulfonates with arylboronic acids.
Cite: Lipeeva A.V. , Shul'ts E.E. , Shakirov M.M. , Bagryanskaya I.Y. , Tolstikov G.A.
Plant coumarins: XIII. Synthesis of 2,3,9-trisubstituted furocoumarins
Russian Journal of Organic Chemistry. 2013. V.49. N3. P.403-411. DOI: 10.1134/S1070428013030159 WOS Scopus РИНЦ OpenAlex
Original: Липеева А.В. , Шульц Э.Э. , Шакиров М.М. , Багрянская И.Ю. , Толстиков Г.А.
Исследование растительных кумаринов xiii. синтез 2,3,9-тризамещенных фурокумаринов
Журнал органической химии (RUSS J ORG CHEM+). 2013. Т.49. №3. С.416-424. РИНЦ
Dates:
Published print: Mar 1, 2013
Published online: Apr 6, 2013
Identifiers:
Web of science: WOS:000317353500015
Scopus: 2-s2.0-84879635437
Elibrary: 20442292
OpenAlex: W2057411734
Citing:
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Web of science 4
Scopus 5
Elibrary 4
OpenAlex 5
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