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A solvent-free amidation of vinylogous esters via direct aziridination
Authors:Emily C. McLaughlin  Anuska ShresthaMadison H. Fletcher  Nathaniel S. SteinauerMin Kyung Shinn  Sabrina M. Shahid
Affiliation:Bard College, 30 Campus Road, Annandale-on-Hudson, NY 12504, United States
Abstract:A microwave-mediated aziridination of α,β-unsaturated ketones and esters through the decomposition of ethyl azidoformate has been developed. When the same atom-economical reaction conditions are applied to cyclic vinylogous esters, N-functionalization at the α-position occurs. Based on NMR analysis, these amidation products appear to be formed from the desired aziridine in moderate to good yields.
Keywords:Aziridination   Ethyl azidoformate   Microwave-mediated synthesis   Vinylogous ester   Amidation
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