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Full-Text Articles in Physical Sciences and Mathematics
Facile And Rapid Synthesis Of Some Novel Polysubstituted Imidazoles By Employing Magnetic Fe_3o_4 Nanoparticles As A High Efficient Catalyst, Bahador Karami, Khalil Eskandari, Abdolmohammad Ghasemi
Facile And Rapid Synthesis Of Some Novel Polysubstituted Imidazoles By Employing Magnetic Fe_3o_4 Nanoparticles As A High Efficient Catalyst, Bahador Karami, Khalil Eskandari, Abdolmohammad Ghasemi
Turkish Journal of Chemistry
Multicomponent, one-pot, highly efficient, and environmentally adapted synthesis of some novel polysubstituted imidazoles by the use of various aldehydes, benzil, aliphatic, and aromatic primary amines and ammonium acetate in the presence of Fe_3O_4 nanoparticles as catalyst under solvent-free condition is explained. A highly efficient role of Fe_3O_4 nanoparticles as catalyst in this synthesis was shown. By this advantage, several polysubstituted imidazoles as pharmaceutical important molecules can be prepared in high yield and high purity. This method is very easy and rapid for the synthesis of imidazole derivatives. All products were deduced from their IR and NMR spectroscopic data. The Fe_3O_4 …
Synthesis And Application Of L-Proline And R-Phenylglycine Derived Organocatalysts For Direct Asymmetric Michael Addition Of Cyclohexanone To Nitroalkenes, Hayri̇ye Nevi̇n Naziroğlu, Abdulkadi̇r Sirit
Synthesis And Application Of L-Proline And R-Phenylglycine Derived Organocatalysts For Direct Asymmetric Michael Addition Of Cyclohexanone To Nitroalkenes, Hayri̇ye Nevi̇n Naziroğlu, Abdulkadi̇r Sirit
Turkish Journal of Chemistry
Novel R-phenylglycine derived organocatalysts were prepared from the reaction of Cbz-R-phenylglycine with indoline, pyrrolidine, or (S)-(-)-2-(diphenylmethyl)pyrrolidine in 3 steps. The asymmetric Michael addition of cyclohexanone to nitroolefins was investigated using R-phenylglycine derivatives along with L-prolinamides as chiral catalysts. The desired products were obtained in excellent yields with enantioselectivities up to 90% ee and diastereomeric ratio up to 98:2 of the syn }addition product.