947504-29-2Relevant academic research and scientific papers
Synthesis of 3-substituted 2-fluoro- And 2,2-difluoroaziridines
Van Hende, Eva,Verniest, Guido,Surmont, Riccardo,De Kimpe, Norbert
, p. 2935 - 2937 (2008/02/07)
A new route for the synthesis of stable 3-alkyl- and 3-aryl-2(,2)-(di) fluoroaziridines was developed by hydride reduction of novel α-bromo- and α-chloro-α(,α)-(di)fluoroketimines and subsequent ring closure of β-fluorinated β-chloro- and β-bromoamines. T
Direct electrophilic α-fluorination of imines: Efficient synthesis of mono-and difluoroimines
Verniest, Guido,Van Hende, Eva,Surmont, Riccardo,De Kimpe, Norbert
, p. 4767 - 4770 (2007/10/03)
(Chemical Equation Presented) A mild and efficient procedure to synthesize α-fluoro- and α,α-difluoroimines was developed. Various N-alkylimines derived from acetophenones were successfully monofluorinated using NFSI (N-fluorobenzenesulfonimide) in a mixture of CH3CN and DMF at 0°C. Alternatively, the same procedure without DMF gave rise to difluorinated imines when performed at room temperature. The obtained α- and α,α-difluorinated imines were subsequently reduced to give the corresponding β-fluoro- and β,β-difluoroamines in good yield.
