Synthesis,characterization, and application of [1-methylpyrrolidin-2-one-SO3H]Cl as an efficient catalyst for the preparation of α-aminophosphonate and docking simulation of ligand bond complexes of cyclin-dependent kinase 2

A sulfonic acid functionalized ionic liquid was designed, synthesized and successfully used as a Brønsted acid catalyst for the one-pot synthesis of α-aminophosphonates containing benzothiazole at room temperature under solvent-free conditions in excellent yields. The advantages of this method are the reusability of the catalyst, high conversion, short reaction time, and simple experimental procedure. A computer modeling and docking simulation of ligand bond complexes of cyclin-dependent kinase 2 are presented. The results indicate that diethyl ((4-(dimethylamino) phenyl) ((6-nitrobenzo[d]thiazol-2-yl) amino)methyl)phosphonate was found to be the best selective inhibitor of cyclin-dependent kinase 2.     

Construction of deletion correcting codes using generalized Reed–Solomon codes and their subcodes

A code is n-deletion correcting if it is possible to correct any n deletion of symbols having occurred in transmission of codewords. In this paper, we present explicit constructions of n-deletion correcting codes for arbitrary values of n using generalized Reed–Solomon codes and their subcodes.      

Scaled‐up,selective and green synthesis of sulfoxides under mild conditions using (CeIII‐MoVI)Ox/aniline hybrid rods as an efficient catalyst

A novel hybrid material, (Ce^III‐Mo^VI)O_x/aniline, with rod‐like morphology is synthesized through a wet chemical method using Mo₃O₁₀(C₆H₅NH₃)₂.2H₂O nanowires as precursor. The synthesized materials are characterized by XRD, XPS, SEM, TEM, FTIR, Raman, UV–Vis, TGA, and elemental analysis. Also, their catalytic activities as a hybrid catalyst are tested in the selective oxidation of sulfides using hydrogen peroxide as a green oxidant. The proposed novel hybrid catalyst shows an excellent performance under green conditions at mild temperature. Furthermore, the scalability of the oxidation reaction is shown by making multi‐gram quantities at optimized conditions.     

Ultrasonic assisted headspace single drop micro-extraction and gas chromatography with nitrogen-phosphorus detector for determination of organophosphorus pesticides in soil

This work describes optimization of headspace single drop micro-extraction for extraction of five organophosphorus pesticides; thionazin, sulfotep, dimethoate, disulfoton and parathion in soil. Ultrasound has also been used successfully to improve and accelerate the extraction of the analytes from the sample. The optimized extraction performance was obtained when the experimental parameters were set as follows; 3.0 μL of octanol as extraction solvent, high ionic strength (20% sodium chloride), 1:1 (w/v) sample dilution with water, extraction temperature at 60 °C for 30 min; applying ultrasound and without any pH adjustment. The optimized method was linear over the calibration range (5–200 and 10–300 for different analytes) with limits of detection of 0.1–2.0 ng g⁻¹. The enrichment factor for OPPs was 1.4–12.7 and the method was also reproducible with the relative standard deviations (RSD%) of 2.1–6.9%.     

Supported palladium oxide nanoparticles in Al-SBA-15 as an efficient and reusable catalyst for the synthesis of pyranopyrazole and benzylpyrazolyl coumarin derivatives via multicomponent reactions

An eco-friendly method for diversity-oriented synthesis of substituted dihydropyrano[2,3-c]pyrazole and benzylpyrazolyl coumarin derivatives has been achieved via one-pot and multicomponent reaction in the presence of PdO/Al-SBA-15 as an efficient and recyclable catalyst in H₂O/EtOH under reflux conditions. The significant merits of this method are wide scope, high yields of the desired products, short reaction times and simple workup procedure. In addition, this nanocatalyst was simply recovered and reused five times without significant loss in catalytic activity and also performance.

Graphical abstract

     

The synthesis of functionalized pyranophenalenones

Abstract  

Protonation of the highly reactive 1:1 intermediate produced in the reaction between alkyl or aryl isocyanides and electron-deficient acetylenic esters with 3-hydroxy-1H-phenalene-1-one leads to a vinylisonitrilium cation, which undergoes an addition reaction with the conjugate base of the 3-hydroxy-1H-phenalene-1-one to produce biologically interesting dialkyl 10-(alkyl or arylamino)-7-oxo-7H,8H-naphtho[1,8-gh]chromene-8,9-dicarboxylates in moderate to fairly good yields at room temperature.     

A New Strategy for the Synthesis of 3-Acyl-coumarin Using Mesoporous Molecular Sieve MCM-41 as a Novel and Efficient Catalyst

3-Acyl-coumarins were obtained in high yields from ortho-hydroxybenzaldehydes and ethyl acetoacetate or ethyl benzoylacetate in acetonitrile in the presence of a catalytic amount of mesoporous molecular sieve MCM-41. 3-Acyl-coumarins were obtained in high yields from ortho-hydroxybenzaldehydes and ethyl acetoacetate or ethyl benzoylacetate in acetonitrile in the presence of a catalytic amount of mesoporous molecular sieve MCM-41.     

Green and Novel Protocol for One-Pot Synthesis of β-Acetamido Carbonyl Compounds Using Mn(bpdo)2Cl2/MCM-41 Catalyst

Aromatic aldehydes were reacted in a one-pot reaction with enolizable ketones, acetonitrile, and acetyl chloride in the presence of Mn(bpdo)₂Cl₂/MCM-41 under reflux condition or at 80 °C to afford the corresponding β-acetamido ketones in good yields.     

Supported Palladium Oxide Nanoparticles in SBA‐15 as a Heterogeneous Catalyst for the Aerobic Oxidation of Alcohols

Palladium nanoparticles were first synthesized through the thermal decomposition method and subsequently immobilized on ordered mesoporous silica material, SBA‐15, to afford PdO/SBA‐15 catalyst. The synthesized catalyst was characterized by X‐ray diffraction, nitrogen adsorption‐desorption measurement, transmission electron microscopy, and inductively coupled plasma atomic emission spectrometry. The catalytic activity was tested for the aerobic oxidation of alcohols. Easy recovery, high yeilds and relatively short reaction times were observed for the mentioned catalyst.     

Synthesis of Benzoxazoles Catalyzed by MCM-41, a Green and Reusable Catalyst

Benzoxazoles can be rapidly and efficiently synthesized from acyl chloride with 2-aminophenols in one simple step, which provided a practical and efficient method for high-throughput synthesis of this important class of heterocyclic compounds.