Stereocontrol of a tertiary hydroxyl group via microbial epoxidation: A facile synthesis of prostaglandin ω-chains
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (12), 1583-1584
- https://doi.org/10.1016/s0040-4039(00)99526-1
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Asymmetric bromolactonization reaction: Synthesis of optically active 2-hydroxy-2-methylalkanoic acids from 2-methylenealkanoic acidsTetrahedron Letters, 1987
- Effects of solvents on the production of epoxides by Nocardia corallina B-276Applied Microbiology and Biotechnology, 1986
- Synthetic Aspects and Applications of Asymmetric EpoxidationPublished by Elsevier ,1985
- On the Mechanism of Asymmetric Epoxidation with Titanium—Tartrate CatalystsPublished by Elsevier ,1985
- Total synthesis of 15-methylprostaglandinsJournal of the American Chemical Society, 1974
- Stereospecific total synthesis of prostaglandins E3 and F3.alpha.Journal of the American Chemical Society, 1971
- 24. A general stereoselective synthesis of olefinsJournal of the Chemical Society, 1959