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 |
|
||
Affiliations |
|
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
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 |