883199-62-0Relevant academic research and scientific papers
Systematic study of halide-induced ring opening of 2-substituted aziridinium salts and theoretical rationalization of the reaction pathways
D'Hooghe, Matthias,Catak, Saron,Stankovic, Sonja,Waroquier, Michel,Kim, Yongeun,Ha, Hyun-Joon,Van Speybroeck, Veronique,De Kimpe, Norbert
experimental part, p. 4920 - 4931 (2010/10/03)
The ring-opening reactions of 2-alkyl-substituted l,1-bis(arylmethyl)- and 1-methyl-1-(l-phenylethyl)aziridinium salts with fluoride, chloride, bromide and iodide in acetonitrile have been, evaluated for the first: time in a systematic way. The reactions
A new approach towards 2-amino-1-aryloxy-3-methoxypropanes from 1-arylmethyl-2-(bromomethyl)aziridines
D'Hooghe, Matthias,Waterinckx, Alex,Vanlangendonck, Tim,De Kimpe, Norbert
, p. 2295 - 2303 (2007/10/03)
1-Arylmethyl-2-(bromomethyl)azirdines were converted into the corresponding 2-(aryloxymethyl)aziridines upon treatment with the appropriate potassium phenoxides in DMF/acetone in excellent yields, followed by regioselective ring opening towards N,N-di(ary
