Highly efficient total synthesis of manoalide and seco-manoalide via Pd(0) catalyzed coupling of allyhalide with CO and 2-silyl-4-stannylfuran
- 1 January 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (10) , 1173-1176
- https://doi.org/10.1016/s0040-4039(00)86680-0
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Total synthesis of E-neomanoalide via Pd(0) catalyzed coupling of allylhalide and α-stannylfuran followed by chemoselective oxygenation of α-silylfuranTetrahedron Letters, 1987
- Luffariellolide, an anti-inflammatory sesterterpene from the marine spongeLuffariella sp.Cellular and Molecular Life Sciences, 1987
- The luffariellins, novel antiinflammatory sesterterpenes of chemotaxonomic importance from the marine sponge Luffariella variabilisThe Journal of Organic Chemistry, 1987
- Total synthesis of manoalideTetrahedron Letters, 1986
- Total synthesis of manoalide and seco-manoalideTetrahedron Letters, 1985
- Some pharmacological observations on marine natural productsTetrahedron, 1985
- Regiospecific synthesis of γ-hydroxybutenolide. Photosensitized oxygenation of substituted 2-trimethylsilylfuranTetrahedron Letters, 1985
- In vitro inactivation of the neurotoxic action of β-bungarotoxin by the marine natural product, manoalideCellular and Molecular Life Sciences, 1984
- Manoalide, an antibiotic sesterterpenoid from the marine sponge (polejaeff)Tetrahedron Letters, 1980
- The regio-specific metalation of heterocyclic compoundsTetrahedron Letters, 1972