1239902-18-1Relevant academic research and scientific papers
Mechanistic study of multi-step nucleophilic substitution for trifluoromethylated styrenes
Rulev, Alexander Yu.,Ushakov, Igor A.,Kondrashov, Evgeniy V.,Muzalevskiy, Vasiliy M.,Shastin, Aleksey V.,Nenajdenko, Valentine G.
body text, p. 945 - 950 (2011/11/05)
The key steps of the reactions of nitrogen nucleophiles with β-halogen-β-trifluoromethylstyrenes have been studied by 19F and 1H NMR monitoring and quantum-chemical calculations. In contrast to the mechanism proposed earlier for nucl
Fragmentation of trifluoromethylated alkenes and acetylenes by N, N -binucleophiles. Synthesis of imidazolines or imidazolidines (Oxazolidines) controlled by substituent
Nenajdenko, Valentine G.,Muzalevskiy, Vasiliy M.,Shastin, Aleksey V.,Balenkova, Elizabeth S.,Kondrashov, Evgeniy V.,Ushakov, Igor A.,Rulev, Alexander Yu.
supporting information; scheme or table, p. 5679 - 5688 (2010/11/19)
The reaction of β-halogeno-β-polyfluoromethylstyrenes with N,N- or N,O-binucleophiles leads to unexpected fragmentation products (imidazolines) or to heterocyclization giving CF3-substituted imidazolidines (N,N-) and oxazolidines (N,O-) depending on aryl substituent. The scope and the reaction mechanism are discussed.
