Short, enantioselective synthesis of (−)-retigeranc acid via [2+3] annulation
- 31 December 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (27) , 3283-3286
- https://doi.org/10.1016/0040-4039(88)85141-4
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Enantiospecific total synthesis of natural (-)-retigeranic acid A and two (-)-retigeranic acid B candidatesThe Journal of Organic Chemistry, 1987
- System oriented design of triquinanes: stereocontrolled synthesis of pentalenic acid and pentaleneneTetrahedron, 1987
- New vinylcyclopropanation methodology and reagents for potential [2 + 3] cyclopentene, dihydrofuran, and pyrroline annulationsThe Journal of Organic Chemistry, 1986
- Total synthesis of (.+-.)-retigeranic acidJournal of the American Chemical Society, 1985
- Total synthesis of (-)-silphiperfol-6-ene and (-)-5-oxosilphiperfol-6-eneJournal of the American Chemical Society, 1984
- Terpenic acids by cyclopentene annulation of exocyclic dienes. Synthesis of the triquinane portion of retigeranic acidThe Journal of Organic Chemistry, 1982
- Stereoselective synthesis of moenocinol and assignment of its carbon-13 nuclear magnetic resonance spectrumThe Journal of Organic Chemistry, 1980
- Synthesis of (-)-acorone and related spirocyclic sesquiterpenesThe Journal of Organic Chemistry, 1975
- Retigeranic acid, a novel sesterterpene isolated from the lichens ofTetrahedron Letters, 1972
- The Favorski˘i Rearrangement of Pulegone DibromideThe Journal of Organic Chemistry, 1965