1142811-89-9Relevant academic research and scientific papers
Efficient synthesis of functionalized aziridinium salts
Chong, Hyun-Soon,Song, Hyun A.,Dadwal, Mamta,Sun, Xiang,Sin, Inseok,Chen, Yunwei
supporting information; experimental part, p. 219 - 221 (2010/04/24)
(Chemical Equation Presented) Various aziridinium salts were efficiently prepared from bromination of a series of backbone substituted N,N-bisubstituted β-amino alcohols and isolated via flash column chromatography. The effect of C-substitution, N-substitution, solvent, leaving group, and counter-anions on formation of the isolable aziridinium salts was investigated. 2009 American Chemical Society.
Stable aziridinium salts as versatile intermediates: Isolation and regio- and stereoselective ring-opening and rearrangement
Song, Hyun A.,Dadwal, Mamta,Lee, Yeseul,Mick, Emily,Chong, Hyun-Soon
supporting information; experimental part, p. 1328 - 1330 (2009/06/30)
Rock trapping and exploration: Aziridinium bromide salts were discovered serendipitously during bromination of N,N-dicarboxymethylated β-amino alcohols. Regiospecific ring-opening and rearrangement of the isolated, surprisingly stable aziridinium salts produces useful molecules including C-functionalized oxomorpholines and α,β-unsaturated amines. 2009 Wiley-VCH Verleg GmbH & Co. KGaA, Weinheim.
