Aromatic nucleophilic substitutions with o- and p-fluoronitrobenzenes in aprotic solvents. Steric effects on the base-catalysed step

The kinetics of the reaction between o- and p-fluoronitrobenzene with n- and iso-propylamine were studied in toluene and DMSO at several amine concentrations and temperatures in the range 30-100°C. The results show that contrary to the previous assumption, primary steric effects due to branching in...

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Autores principales: Nudelman, N.S., Cerdeira, S.
Formato: JOUR
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_1472779X_v_n5_p695_Nudelman
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