Publication | Closed Access
Diastereoselective Synthesis of α-Quaternary Aziridine-2-carboxylates via Aza-Corey–Chaykovsky Aziridination of <i>N</i>-<i>tert</i>-Butanesulfinyl Ketimino Esters
71
Citations
64
References
2015
Year
α-Quaternary Aziridine-2-carboxylatesDerivativesAvailable PrecursorsBiochemistryDiastereoselective AziridinationNatural SciencesEngineeringDiversity-oriented SynthesisDiastereoselective SynthesisOrganic ChemistryAza-corey–chaykovsky AziridinationN-tert-butanesulfinyl Ketimino EstersChemistryNatural Product SynthesisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
A general, scalable, and highly diastereoselective aziridination of N-tert-butanesulfinyl ketimino esters is described. The methodology has been utilized to provide straightforward access to previously unobtainable, biologically relevant α-quaternary amino esters and derivatives starting from readily available precursors.
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