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Synthetic transformations of higher terpenoids: V. 2-Methyl-4,5-dioxo-3-ethoxycarbonyl-4,5-dihydroindole, a new dienophile. Synthesis of indoloterpenes from levopimaric acid Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 2000, Volume: 36, Number: 11, Pages: 1623-1633 Pages count : 11
Authors Chernov S.V. 1 , Shults E.E. 1 , Shakirov M.M. 1 , Gatilov Yu.V. 1 , Bagryanskaya I.Yu. 1 , Tolstikov G.A. 1
Affiliations
1 (Scopus) Vorozhtsov Novosibirsk Inst. of O., Siberian Division, Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation

Abstract: 2-Methyl-4,5-dioxo-3-ethoxycarbonyl-4,5-dihydroindol is an active dienophile that via [4+2]-cycloaddition to the levopimaric acid and to the cyclopentadiene affords indole alkaloids of new structural types.
Cite: Chernov S.V. , Shults E.E. , Shakirov M.M. , Gatilov Y.V. , Bagryanskaya I.Y. , Tolstikov G.A.
Synthetic transformations of higher terpenoids: V. 2-Methyl-4,5-dioxo-3-ethoxycarbonyl-4,5-dihydroindole, a new dienophile. Synthesis of indoloterpenes from levopimaric acid
Russian Journal of Organic Chemistry. 2000. V.36. N11. P.1623-1633. WOS Scopus РИНЦ
Identifiers:
Web of science: WOS:000168791600012
Scopus: 2-s2.0-0034310420
Elibrary: 13336762
Citing:
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Scopus 2
Web of science 2
Elibrary 2