A new synthesis of the vernolepin a-ring
- 31 December 1974
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 15 (18), 1713-1715
- https://doi.org/10.1016/s0040-4039(01)82561-2
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Model studies directed toward the total synthesis of vernolepin: construction of the α-methylene-δ-lactone portion of vernolepin.Tetrahedron Letters, 1973
- Acid-catalyzed rearrangement of tricyclo[4.4.0.2,7]decan-3-olsThe Journal of Organic Chemistry, 1972
- α-Hydroxymethylation of γ- and δ-lactones: a new synthesis of α-methylene-γ-butyrolactonesJournal of the Chemical Society, Chemical Communications, 1972
- New methods for carbocyclic synthesis applicable to the gibberellic acids. Steroselective introduction of the angular vinyl grouping and pinacolic cyclization of keto aldehydesJournal of the American Chemical Society, 1971
- Tumor inhibitors. XLVI. Vernolepin, a novel sesquiterpene dilactone tumor inhibitor from Vernonia hymenolepisThe Journal of Organic Chemistry, 1969
- Isolation of ketone enolates as trialkylsilyl ethersJournal of the American Chemical Society, 1968
- Tumor inhibitors. XXXI. Vernolepin, a novel elemanolide dilactone tumor inhibitor from Vernonia hymenolepisJournal of the American Chemical Society, 1968
- Preparation of cis-Hexahydroindane-8-carboxylic AcidThe Journal of Organic Chemistry, 1961