PRACTICAL SYNTHESIS OF (+)-9(O)-METHANO-Δ6(9α)-PGI1. THE HIGHLY POTENT CARBON ANALOG OF PROSTACYCLIN
- 5 April 1984
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 13 (4) , 579-582
- https://doi.org/10.1246/cl.1984.579
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Synthesis of 9(0)-Methano-Δ6(9α)-PGI1: The highly potent carbon analog of prostacyclinTetrahedron Letters, 1983
- Regiocontrolled conversion of α,β-unsaturated ketones to olefins allylsilanes: synthesis of -9(0)-methano-Δ6(9α)-PGI1Tetrahedron Letters, 1983
- Methylenation of carbonyl compounds with ZnCH2Br2TiCl4. Application to gibberellinsTetrahedron Letters, 1982
- Diisobutylaluminum 2,6-di-tert-butyl-4-methylphenoxide. Novel stereoselective reducing agent for prostaglandin synthesisThe Journal of Organic Chemistry, 1979
- Stereospecific total synthesis of gibberellic acid. A key tricyclic intermediateJournal of the American Chemical Society, 1978
- Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chlorideThe Journal of Organic Chemistry, 1978