RESUMO
A highly efficient and air-, thermal-, and moisture-stable nickel-based catalyst with excellent magnetic properties supported on silica-coated magnetic Fe3O4 nanoparticles was successfully synthesized. It was well characterized by Fourier transform infrared spectroscopy, powder X-ray diffraction, transmission electron microscopy, field emission scanning electron microscopy, thermogravimetric analysis, dynamic light scattering (DLS), X-ray photoelectron spectroscopy, vibration sample magnetometry, energy-dispersive X-ray analysis, inductively coupled plasma analysis, and nitrogen adsorption-desorption isotherm analysis. The Suzuki-Miyaura coupling reaction between aryl carbamates and/or sulfamates with arylboronic acids was selected to demonstrate the catalytic activity and efficiency of the as-prepared magnetic nanocatalyst. Using the mentioned heterogeneous nanocatalyst in such reactions generated corresponding products in good to excellent yields in which the catalyst could easily be recovered from the reaction mixture with an external magnetic field to reuse directly for the next several cycles without significant loss of its activity.
RESUMO
Several straightforward and practical processes have been established for the construction of 2-aminothiazoles, 1,3-thiazoles and 1,3-selenazoles from aryliodoazides. These strategies successfully proceed with a wide spectrum of substituted thioamides and its derivatives producing the resulting five-membered heterocycles obtained in satisfactory yields. The unique features of these protocols are operational simplicity and highly functional group tolerance, which make them convenient and practical routes for the preparation of various libraries of 2-aminothiazoles, 1,3-thiazoles, and 1,3-selenazoles.
