Synthesis of 5‐substituted 1H‐tetrazoles using a recyclable heterogeneous nanonickel ferrite catalyst

An efficient method was developed for the [2 + 3] cycloaddition of sodium azide with nitriles to afford 5‐substituted 1H‐tetrazoles using nanonickel ferrite (NiFe₂O₄) as an effective heterogeneous catalyst in dimethylformamide. The main advantages of this method are high yields, simple methodology and easy work‐up. The catalyst can be recovered and reused for several cycles with predictable activity. Copyright © 2015 John Wiley & Sons, Ltd.     

H14[NaP5W29MoO110]: a Novel and Useful Catalyst for Aminolysis of Epoxides with Amines under Solvent-Free Conditions

A simple and efficient method has been developed for the synthesis of β-amino alcohols by ring opening of epoxides in the presence of a catalytic amount of H14[NaP5W29MoO110] at room temperature under solvent-free conditions. The reaction works well for both aromatic and aliphatic amines.     

TBHP/R4N+X– promoted hydroaroylation of dialkyl azodicarboxylates with methyl arenes,aldehydes, aryl methanols and arylmethyl chlorides

Efficient TBHP/R₄N⁺X^– promoted hydroaroylations of dialkyl azo-1,2-dicarboxylates with methyl arenes, aldehydes, aryl methanols and arylmethyl chlorides are described. These oxidation/oxygenation and hydroaroylation processes were carried out by tert-butyl hydroperoxide as terminal oxidant/oxygen source, and were catalyzed by tetrabutylammonium bromide and tricaprylmethylammonium chloride as the driving force. During this investigation, all these hydroaroylating sources were found to be highly efficient reagents without the need of any transition-metal.     

Immobilized triazine bis[mercapto amine] complexes of Pd(0) anchored nickel ferrite as a nanocatalyst for C–C coupling reaction

Immobilized triazine bis[mercapto amine] complexes of Pd(0) (NiFe₂O₄@TABMA-Pd(0)) was easily synthesized and applied as highly efficient and versatile nanocatalyst for the synthesis of various trans stilbenes with high performance for the Heck coupling reaction of several types of aryl halides under thermal conditions. In short reaction time, excellent yields of trans stilbene derivatives have been achieved using NiFe₂O₄@TABMA-Pd(0) catalyst.     

Improving of Anticancer Activity and Solubility of Cisplatin by Methylglycine and Methyl Amine Ligands Against Human Breast Adenocarcinoma Cell Line

Methylglycine, also known sarcosine, is dramatically used in drug molecules and its metal complexes can interact to DNA and also do cleavage. Hence, to study the influence of methylglycine ligand on biological behavior of metal complexes, two water-soluble platinum (II) complexes with the formula cis-[Pt(NH₃)₂(CH₃-gly)]NO₃ and cis-[Pt(NH₂-CH₃)₂(CH₃-gly)]NO₃ (where CH₃-gly is methylglycine) have been synthesized and characterized by spectroscopic methods, molar conductivity measurements, and elemental analyzes. The anticancer activity of synthesized complexes was tested against human breast adenocarcinoma cell line of MCF7 using MTT assay and results showed excellent anticancer activity with Cc₅₀ values of 126 and 292 μM after 24 h incubation time, for both complexes of cis-[Pt(NH₃)₂(CH₃gly)]NO₃ and cis-[Pt(NH₂-CH₃)₂(CH₃gly)]NO₃, respectively. Also, the interaction between Pt(II) complexes with calf thymus DNA was extensively studied by means of absorption spectroscopy, fluorescence titration spectra displacement with ethidium bromide (EtBr), and circular dichroism studied in Tris-buffer. The obtained spectroscopic results revealed that two complexes can bind to highly polymerized calf thymus DNA cooperatively and denature at micromolar concentrations. The fluorescence data indicate that quenching effect for cis-[Pt(NH₃)₂(CH₃gly)]NO₃ (K_sv?=?9.48 mM^?1) was higher than that of cis-[Pt(NH₂-CH₃)₂(CH₃gly)]NO₃ (K_sv?= 1.98 mM^?1). These results were also confirmed by circular dichrosim spectra. Consequently, docking data showed that cis-[Pt(NH₃)₂(CH₃gly)]NO₃ with more interaction energy binds on DNA via groove binding which is more compatible with experimental results.

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Graphical Abstract ? Two anticancer Pt(II) complexes, cis-[Pt(NH₃)₂(CH₃gly)]NO₃ and cis-[Pt(NH_2?CH₃)₂(CH₃gly)]NO₃, have been synthesized and interacted with calf thymus DNA. Improving solubility of these compounds reduce side effects and increase anticancer activity against human breast cell line. Modes of binding have been studied by electronic absorption, fluorescence, and CD measurements. Results show that both Pt(II) complexes can interact to DNA via groove binding.

     

Electrochemical Oxidation of Nortriptyline and Its Voltammetric Sensing at a Carbon Ionic Liquid Electrode

The electrochemical oxidation of nortriptyline at a carbon ionic liquid electrode (CILE) was investigated. Nortriptyline is electrochemically inactive on conventional electrodes but CILE exhibited excellent electrocatalytic activity toward oxidation of nortriptyline with the well-defined anodic peak at 860 mV. This characteristic was attributed to the outstanding conductivity and electrocatalytic effect of the ionic liquid, 1-octylpyridinum hexaflourophosphate, used as a binder in the construction of the electrode. The influence of experimental parameters such as pH and sweep rate was also studied. The quantitative determination of nortriptyline was performed using differential pulse voltammetry technique. Under selected conditions the anodic peak current was linear to nortriptyline concentration in the ranges of 4.8 × 10^–6 to 2.4 × 10^–5 M and 2.4 × 10^–5 to 6.4 × 10^–5 M, with correlation coefficients of 0.9992 and 09949, respectively. The detection limit was 3 × 10^–7 M.