76336-94-2Relevant articles and documents
An amine-promoted aziridination of chalcones
Shen, Yu-Mei,Zhao, Mei-Xin,Xu, Jiaxi,Shi, Yian
, p. 8005 - 8008 (2006)
(Chemical Equation Presented) Without protection: α-Keto aziridines have been formed in a novel amine-promoted direct aziridination of chalcones using an aminimide generated in situ from a tertiary amine and O-mesitylenesulfonylhydroxylamine (MSH) in the
Efficient aziridination of α,β-unsaturated ketones with O-(2,4-dinitrophenyl)-hydroxylamine
Wang, Jin-Jia,Lao, Jin-Hua,Li, Xue-Ming,Lu, Rui-Jiong,Miao, Hui,Yan, Ming
experimental part, p. 1577 - 1584 (2012/05/05)
The aziridination of α,β-unsaturated ketones with O-(2,4-dinitrophenyl)-hydroxylamine and tertiary amine was developed. trans-Aziridines were obtained exclusively in good yields. The reaction is proposed to occur via an aminimide intermediate. Copyright T
N-amino-N-methylmorpholinium salts: Highly active aziridination reagents for chalcones
Armstrong, Alan,Carbery, David R.,Lamont, Scott G.,Pape, Andrew R.,Wincewicz, Richard
, p. 2504 - 2506 (2008/02/11)
A highly effective aziridination reagent, based on N-methylmorpholine, is reported which effects rapid conversion of chalcones to N-unfunctionalised aziridines at room temperature. Georg Thieme Verlag Stuttgart.