Publication | Closed Access
Flexible and Chemoselective Oxidation of Amides to α-Keto Amides and α-Hydroxy Amides
141
Citations
48
References
2017
Year
Chemical EngineeringMedicinal ChemistryBioorganic ChemistryEngineeringBiochemistryChemoselective OxidationValuable Motifsα-Hydroxy AmidesDiversity-oriented Synthesisα-Keto AmidesNatural SciencesOrganic ChemistryCatalysisStereoselective SynthesisChemistrySynthetic ChemistryEnantioselective Synthesis
A suite of flexible and chemoselective methods for the transition-metal-free oxidation of amides to α-keto amides and α-hydroxy amides is presented. These highly valuable motifs are accessed in good to excellent yields and stereoselectivities with high functional group tolerance. The utility of the method is showcased by the formal synthesis of a potent histone deacetylase inhibitor.
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