Publication | Open Access
Azidation of β-Keto Esters and Silyl Enol Ethers with a Benziodoxole Reagent
170
Citations
28
References
2013
Year
Chemical Engineeringβ-Keto EstersEfficient AzidationEngineeringBenziodoxole ReagentOrganic ChemistrySilyl Enol EthersCatalysisZinc CatalystChemistryAsymmetric CatalysisEnantioselective SynthesisCatalytic Synthesis
The efficient azidation of β-keto esters and silyl enol ethers using a benziodoxole-derived azide transfer reagent is reported. The azidation of cyclic β-keto esters could be achieved in up to quantitative yields in the absence of any catalyst. In the case of less reactive linear β-keto esters and silyl enol ethers, complete conversion and good yields could be obtained by using a zinc catalyst.
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