Publication | Closed Access
Intramolecular Rearrangement of α-Azidoperoxides: An Efficient Synthesis of <i>tert</i>-Butyl Esters
14
Citations
37
References
2015
Year
Intramolecular RearrangementSimple Organic BaseBiochemistryUnprecedented Intramolecular RearrangementEngineeringNatural SciencesDiversity-oriented SynthesisAlkene MetathesisOrganic ChemistryCatalysisChemistryAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringOne-pot Methodology
An unprecedented intramolecular rearrangement of α-azidoperoxides, promoted by simple organic base to provide tert-butyl esters, has been presented. Further, a one-pot methodology consisting of in situ generation of the α-azidoperoxides from corresponding aldehydes followed by base-promoted rearrangement to obtain the desired ester has also been executed. Relevant mechanistic studies, to provide the proof for intramolecular alkoxy transfer, are investigated.
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