A method for the oxidation of , -1,2-diols to α-hydroxy ketones without carbon-carbon cleavage
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. The Cleavage of cis- and trans-1,2-Dimethyl-1,2-cyclopentanediol by Chromic Acid
2. New and highly effective method for the oxidation of primary and secondary alcohols to carbonyl compounds
3. Oxidation of primary and secondary alcohols to carbonyl compounds using dimethyl sulfoxide--chlorine complex as reagent
4. Improved sythetic routes to prostaglandins utilizing sulfide-mediated oxidation of primary and secondary alcohols
5. A method for selective conversion of allylic and benzylic alcohols to halides under neutral conditions
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1. Serendipitous discovery of Pd-catalyzed intramolecular cyclization of ortho-bromo(hetero)aryl-substituted (hetero)aryl-1,2-diketones: Applications in the synthesis of carba- and heterocyclic benzoin derivatives;Tetrahedron;2023-04
2. Efficient and eco-friendly oxidative cleavage of C–C bonds of 1,2-diols to ketones: electrochemistry vs thermochemistry;Organic Chemistry Frontiers;2022
3. Facile one-pot synthesis of ketones from primary alcohols under mild conditions;New Journal of Chemistry;2021
4. Oxidations and Reductions;Applied Organic Chemistry;2020-12-11
5. Reversible PCET and Ambient Catalytic Oxidative Alcohol Dehydrogenation by {V=O} Perfluoropinacolate Complexes;Inorganic Chemistry;2020-10-29
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