75872-57-0Relevant academic research and scientific papers
Tertiary Amine Promoted Aziridination: Preparation of NH-Aziridines from Aliphatic α,β-Unsaturated Ketones
Armstrong, Alan,Pullin, Robert D. C.,Scutt, James N.
supporting information, p. 151 - 155 (2015/12/26)
trans-NH-Aziridines were prepared from aliphatic α,β-unsaturated ketones using a tertiary amine promoted reaction via in situ generated N,N-ylides. Through use of modified conditions the reaction proved to be applicable for the diastereoselective aziridination of a range of enolisable aliphatic α,β-unsaturated ketones of varying substitution patterns.
Reactivite photochimique des alkylamino-2 cyclohexene-2 ones. Formation de cetoaziridines
Cossy, J.,Pete, J. P.
, p. 2947 - 2948 (2007/10/02)
Un acces a des cetoaziridines par photolyse d'alkylamino-2 cyclohexene-2 ones est possible pour les derives N-benzyles.
