Journal
ORGANIC LETTERS
Volume 17, Issue 22, Pages 5614-5617Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b02838
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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 alpha-quaternary amino esters and derivatives starting from readily available precursors.
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