Publication | Closed Access
TEMPO‐Mediated Oxidative Deformylation of Aldehydes: Applications in the Synthesis of Polyketide Fragments
12
Citations
10
References
2017
Year
EngineeringSynthetic ProtocolOrganic ChemistryChemistryPolyketide FragmentsSynthetic ChemistryPrecursor AldehydeDerivativesRadical (Chemistry)Diversity-oriented SynthesisCatalysisNatural Product SynthesisTempo AdductsEnantioselective SynthesisBiomolecular EngineeringNatural SciencesPolymer ReactionDeoxygenationOxidative Deformylation
A TEMPO‐mediated oxidative deformylation of aldehydes is reported that yields the TEMPO adducts, which can be further oxidized to the corresponding ketones. The focus of this work was on the optimization of a synthetic protocol for use in natural product synthesis, specifically for the preparation of chiral backbones with 1,2‐oxo functionalization found in polyketide antibiotics. In addition, the oxidative deformylation was combined with the oxidation of the alcohol to the precursor aldehyde in a one‐pot protocol.
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