Access to NH-Aziridine-2-Carboxamides through Davidsen Acylimidodicarbonate Activation

Comptes Rendus Chimie 2019
Jekaterīna Ivanova, Boriss Štrumfs, Raivis Žalubovskis

Acylimidodicarbonates obtained from aziridine-2-carboxamides through Davidsen bis-Boc activation react with amine nucleophiles under mild conditions to form tertiary aziridine-2-carboxylic acid amides. NH aziridine-2-carboxylic acid amides were obtained by hydrogenolythic deprotection of N-Cbz derivatives.

Keywords
Acylimidodicarbonates, Aziridine-2-carboxamides, Aziridines, Davidsen activation, Nucleophiles
DOI
10.1016/j.crci.2019.03.001
Hyperlink
https://www.sciencedirect.com/science/article/pii/S1631074819300402

Ivanova, J., Štrumfs, B., Žalubovskis, R. Access to NH-Aziridine-2-Carboxamides through Davidsen Acylimidodicarbonate Activation. Comptes Rendus Chimie, 2019, Vol. 22, No. 4, pp.283-293. ISSN 1631-0748. Available from: doi:10.1016/j.crci.2019.03.001

Publication language
English (en)