Dowex-50W-hyodrgen ion exchange resin was used as a reusable catalyst for the synthesis of oxazoline, imidazoline and thiazoline derivatives through condensation reaction between arylnitriles and 2-aminoalcohol, ethylenediamine or 2-aminoethanthiol. This process provides several advantages such as excellent yields of the products, simple operation, convenient separation and inexpensive and recy...

A feasible "NOSE" (nanoparticles-catalyzed organic synthesis enhancement) protocol has been developed for N,N-diformylation of bisuracil derivatives using nano-Al2O3 rods as an efficient, inexpensive, and recyclable catalyst under solvent-free reaction condition at 40°C. The catalyst was reused up to the 4th cycle without affecting the rate and yield of the N,N-diformylation products appreciably.

The use of a recyclable phase transfer catalyst, SiO2-PEG-ImBr, is demonstrated in a simple and highly efficient synthesis of phenacyl derivatives by nucleophilic substitution reaction of phenacyl halides with different anions in water. Advantages of this system are easy work-up, moderate to good yields, and recyclable catalyst. The catalyst can be recycled and reused several times with no loss...

A new BiCl3-loaded montmorillonite K10 catalyst has been prepared by solid dispersion method and was characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and cyclic voltammetry (CV) measurements. BiCl3 loaded K10 (BiCl3-K10) has been used as solid acid catalyst for the synthesis of azine derivatives from benzophenone hydrazone and ketones/aldehydes by ...

Well-dispersed palladium (0) nanoparticles stabilized with phosphonium based ionic liquid were synthesized conveniently and fully characterized. A catalyst system comprising of the Pd(0) nanoparticles and a base was found to be recyclable and efficient for the aminocarbonylation reaction of aryl iodide in ionic liquid media. In the presence of potassium tert-butyloxide, for the relatively stabl...

Recyclable ( -p-cymene)-ruthenium(II) 2-naphthylazo-p-methylphenolate catalyst of formulation [RuCl( -pcymene)(L)] (where L = mono anionic 2-naphthylazo-p-methylphenolate ligand) is shown to be an efficient catalyst for transfer hydrogenation of a wide range of alkyl and aryl ketones in the presence of 2-propanol and KOH.

A novel and green approach for efficient and rapid synthesis of biologically active polyhydroquinoline derivatives via unsymmetric Hantzsch reaction using nanorods Vanadatesulfuric acid (VSA NRs) as a new and recyclable catalyst under solvent-free conditions was reported. The catalyst was characterized by FT-IR, XRD, XRF and TEM analysis. The present method offers several advantages such as sim...

cui nanoparticles as an expedient and recyclable catalyst for the synthesis of n-cyclohexyl-3-aryl-quinoxaline-2-amines in ethanol via a multi-component reaction are established. the products were separated from the catalyst simply by filtration. the catalyst could be recycled and reused for several times without noticeably decreasing the catalytic activity.

Here, we report insights into the new recyclable catalyst 1, (DMAP·saccharin). The DMAP·saccharin-catalysed acylation of alcohols has been successfully carried out more than 8 times. Only 1 mol% of catalyst 1 efficiently promotes acylation with almost equimolar amounts of acid anhydrides, under both base-free and solvent-free conditions.

Cellulose/KI is a very active, selective, stable, and recyclable catalyst for the cycloaddition reactions of CO(2) and epoxides due to the excellent synergetic effect of cellulose and KI. It is found that the hydroxyl groups on the vicinal carbons of cellulose play a key role for the very high efficiency of the catalyst.