159562-65-9Relevant academic research and scientific papers
The CF3CH2O- adducts of α-nitro-β-(2,2,2-trifluoroethoxy)stilbene and β-methoxy-α-nitrostilbene, and the MeO- adduct of β-methoxy-α-nitrostilbene. Kinetics of competition between protonation and acid catalyzed a
Bernasconi, Claude F.,Schuck, David F.,Ketner, Rodney J.,Eventova, Irina,Rappoport, Zvi
, p. 2719 - 2725 (2007/10/02)
The reaction of aqueous acids with the CF3CH2O- adduct, Ph(OCH2CF3)2CC(Ph)=NO2-, of α-nitro-β-(2,2,2-trifluoroethoxy)stilbene leads virtually exclusively to the corres
Kinetic analysis of elementary steps in nucleophilic vinylic substitution reactions of α-nitro-β-X-stilbenes (X = OCH2CF3, OCH3, NO2) with various nucleophiles.
Bernasconi, Claude F.,Schuck, David F.,Ketner, Rodney J.,Weiss, Minda,Rappoport, Zvi
, p. 11764 - 11774 (2007/10/02)
Rate constants of elementary steps in the addition-elimination mechanism of nucleophilic vinylic substitutions (SNV) were determined by studying the following reactions in 50% Me2SO-50% water at 20 °C: (1) α-nitro-β-(2,2,2-trifluoroethoxy)stilb
