STEREOSELECTIVE SYNTHESIS OF MESO(OR ERYTHRO) 1,3-DIOLS FROM β-HYDROXYKETONES
- 5 November 1980
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 9 (11), 1415-1418
- https://doi.org/10.1246/cl.1980.1415
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Stereoselective reduction of β-keto esters with zinc borohydride. stereoselective synthesis ofTetrahedron Letters, 1980
- Synthesis of the polyether antibiotic monensin. 3. Coupling of precursors and transformation to monensinJournal of the American Chemical Society, 1980
- Synthesis of the polyether antibiotic monensin. 2. Preparation of intermediatesJournal of the American Chemical Society, 1980
- Synthesis of the polyether antibiotic monensin. 1. Strategy and degradationsJournal of the American Chemical Society, 1980
- Stereocontrol in the synthesis of acyclic systems: applications to natural product synthesisTetrahedron, 1980
- Stereoselective aldol condensations via boron enolatesJournal of the American Chemical Society, 1979
- "Phosphate extension". A strategem for the stereoselective functionalization of acyclic homoallylic alcoholsJournal of the American Chemical Society, 1977
- 1,3-asymmetric induction—VITetrahedron, 1974
- Action des organomagnésiens sur les composés β-dicarbonylés V. Synthèses de β-diols bitertiaires à partir de β-hydroxycétones. Induction asymétrique 1-3Canadian Journal of Chemistry, 1971
- Studies in stereochemistry. XXXVIII. Open-chain vs. cyclic models for 1,3-asymmetric induction in addition reactionsJournal of the American Chemical Society, 1968