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

Citation
Sv. Chernov et al., 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, RUSS J ORG, 36(11), 2000, pp. 1623-1633
Citations number
28
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
ISSN journal
10704280 → ACNP
Volume
36
Issue
11
Year of publication
2000
Pages
1623 - 1633
Database
ISI
SICI code
1070-4280(200011)36:11<1623:STOHTV>2.0.ZU;2-W
Abstract
2-Methyl-4,5-dioxo-3-ethoxycarbonyl-4,5-dihydroindol is an active dienophil e that via [4+2]-cycloaddition to the levopimaric acid and to the cyclopent adiene affords indole alkaloids of new structural types.