Three-component synthesis of N-sulfonylformamidines in the presence of magnetic cellulose supported N-heterocyclic carbene-copper complex,as an efficient heterogeneous nanocatalyst

A cellulose based magnetic nanocomposite possessing NHC-Cu Complex has been synthesized and characterized. It was then applied as a highly active catalyst in one-pot three-component reaction of sulfonyl azides, secondary amines and triethylamine to afford N-sulfonylformamidines. Copper catalyzed oxidative transformation of C-N bond of triethylamine is a key step to give desired products. In contrast with the good reactivity of the conventional secondary amines, aromatic amines and NH containing heteroaromatics had no activity in these reactions. Moreover, the used nanocatalyst which could be recovered by external magnet, showed reasonable catalytic activity for several times.     

Synthesis of Betti base derivatives catalyzed by nano-CuO-ionic liquid and experimental and quantum chemical studies on corrosion inhibition performance of them

Research on Chemical Intermediates - In this research, for the first time, aminonaphthol derivatives were introduced as efficient corrosion inhibitors. A linear polarization method was employed to...     

Synthesis and calcium channel antagonist activity of new symmetrical and asymmetrical 4-[2-chloro-2-(4-chloro-6-methyl-2-oxo-2H-pyran-3-yl)vinyl]-substituted 1,4-dihydropyridines

New symmetrical 4-[2-chloro-2-(4-chloro-6-methyl-2-oxo-2H-pyran-3-yl)vinyl]-substituted 1,4-di-hydropyridines were synthesized in moderate to good yields via the modified Hantzsch reaction of β-dicarbonyl compounds with (Z)-3-chloro-3-(4-chloro-6-methyl-2-oxo-2H-pyran-3-yl)acrolein in the presence of an excess amount of NH₄OAc. Also, the reaction of β-dicarbonyl compounds with (Z)-3-chloro-3-(4-chloro-6-methyl-2-oxo-2H-pyran-3-yl)acrolein in the presence of enamino esters and ketones was performed, and asymmetrical 4-[2-chloro-2-(4-chloro-6-methyl-2-oxo-2H-pyran-3-yl)vinyl]-substituted 1,4-dihydropyridines were obtained in moderate to good yields at room temperature. The calcium channel blocking activity of these compounds was assessed. They demonstrated moderate to weak effects, although one compound had a comparable effect (IC₅₀ =1.40×10⁻⁷ M) with respect to the reference drug Nifedipine.     

Enhanced catalytic performance of copper iodide in 1,2,3-triazole-imidazole hybrid synthesis,and evaluation of their anti-cancer activities along with optical properties besides 1H-tetrazole-imidazole hybrids

New triazole-imidazole and tetrazole-imidazole hybrids were obtained using 2,4,5-triaryl-1-(4-aminophenyl) imidazoles by copper-catalyzedazide-alkyne cycloaddition (CuAAC) and Ugi-azidefour-component(UA-4CRs) process. The synthesis of triazole hybrids was performed in the presence of new copper-incorporated white sandstone nanocatalyst, which was fully characterized by different methods. The construction of newly prepared hybrids was confirmed by spectroscopic techniques. Some of these compounds were evaluated for their anti-cancer properties against MCF-7 cancer cell lines. The absorption and emission parameters of the triazole- and tetrazole-substituted imidazoles were also investigated and compared with each other.     

Synthesis of fused pyrimidone derivatives of 4-pyrones from the acetates of Baylis–Hillman adducts

A series of fused pyrimidone derivatives of 4-pyrones was synthesized by conversion of the acetates of Baylis−Hillman adducts obtained from 2-formyl-4-pyrones with 2-aminopyridine and 2-aminothiazole.