Preparation of chiral diols by the osmium-catalysed, indirect anodic oxidation of olefins
- 1 September 1992
- journal article
- Published by Springer Nature in Journal of Applied Electrochemistry
- Vol. 22 (9) , 810-816
- https://doi.org/10.1007/bf01023722
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Preclusion of the “second cycle” in the osmium-catalyzed asymmetric dihydroxylation of olefins leads to a superior processTetrahedron Letters, 1990
- Highly enantioselective dihydroxylation of trans-disubstituted and monosubstituted olefinsThe Journal of Organic Chemistry, 1989
- Documenting the scope of the catalytic asymmetric dihydroxylationTetrahedron Letters, 1989
- Asymmetric dihydroxylation via ligand-accelerated catalysisJournal of the American Chemical Society, 1988
- Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatizationJournal of the American Chemical Society, 1987
- Osmium tetraoxide cis hydroxylation of unsaturated substratesChemical Reviews, 1980
- The electrochemical reduction of BenzaldehydeElectrochimica Acta, 1980
- Oxidation of benzpinacol in alkaline solutionJournal of the American Chemical Society, 1969
- .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and aminesThe Journal of Organic Chemistry, 1969
- Oxidation of Olefins by Ferricyanide Using Osmium Tetroxide CatalystI&EC Product Research and Development, 1968