A method for the oxidation of , -1,2-diols to α-hydroxy ketones without carbon-carbon cleavage
- 1 January 1974
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 15 (3) , 287-290
- https://doi.org/10.1016/s0040-4039(01)82195-x
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Improved sythetic routes to prostaglandins utilizing sulfide-mediated oxidation of primary and secondary alcoholsThe Journal of Organic Chemistry, 1973
- Oxidation of primary and secondary alcohols to carbonyl compounds using dimethyl sulfoxide--chlorine complex as reagentTetrahedron Letters, 1973
- A method for selective conversion of allylic and benzylic alcohols to halides under neutral conditionsTetrahedron Letters, 1972
- New and highly effective method for the oxidation of primary and secondary alcohols to carbonyl compoundsJournal of the American Chemical Society, 1972
- New methods for carbocyclic synthesis applicable to the gibberellic acids. Steroselective introduction of the angular vinyl grouping and pinacolic cyclization of keto aldehydesJournal of the American Chemical Society, 1971
- Pummerer rearrangements of sulfonium saltsJournal of the American Chemical Society, 1969
- The Cleavage of cis- and trans-1,2-Dimethyl-1,2-cyclopentanediol by Chromic AcidJournal of the American Chemical Society, 1962
- The Stereochemistry of the Hydrogenolysis of 1,2-Diphenyl-1,2-propanediolJournal of the American Chemical Society, 1959
- Optisch aktive Methyl‐ und Äthyl‐benzoineBerichte der deutschen chemischen Gesellschaft (A and B Series), 1937