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Transition metal-free oxidative ortho-acylation of phenols with N-heteroarylmethanes via double C–H activation
18
Citations
63
References
2016
Year
Chemical EngineeringMetal-free ConditionsEngineeringAlkene MetathesisPlausible MechanismDirect Oxidative AcylationOrganic ChemistryOrganometallic CatalysisCatalysisDouble C–h ActivationChemistryMolecular Catalysis
The direct oxidative acylation of phenols with <italic>N</italic>-heteroarylmethanes <italic>via</italic> sp<sup>3</sup>C–H and sp<sup>2</sup>C–H double activation was achieved under metal-free conditions. The reaction proceeds in a facile I<sub>2</sub>/DMSO/O<sub>2</sub> system regio-selectively to produce valuable (2-hydroxyphenyl)arylmethanones. A plausible mechanism was proposed.
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