Application of Heteropolyacids as Heterogeneous and Recyclable Catalysts for One-Pot Synthesis of 3-Cyanopyridine Derivatives

A simple, clean and environmentally benign route to the synthesis of 3-cyanopyridines is described via a one-pot multi-component reaction of 3,4-dimethoxyacetophenone, malonitrile or ethylcyanoacetate, aldehyde and ammonium acetate using heteropolyacids as heterogeneous and recyclable catalysts in very good yields.     

Synthesis of Isobenzofuran-1(3H)-ones with the Aid of Silica-Supported Preyssler Nanoparticles

Silica-supported Preyssler nanoparticles appear to be a new and efficient solid acid catalyst for an economical, and environmentally benign one-pot synthesis of 3-substituted phthalides.     

Highly effective and regioselective Michael addition of indoles to α,β-unsaturated ketones promoted by pentafluorophenylammonium triflate

A simple, inexpensive, environmentally friendly and efficient route for Michael addition of indoles to α,β-unsaturated ketones using pentafluorophenylammonium triflate (PFPAT) as a catalyst is described. Various indole derivatives were synthesized in good to excellent yields. The preparation of PFPAT catalyst from simple and readily available starting materials makes this method more affordable.     

1,3-Migration of Trimethylsilyl Group from Carbon to Oxygen in Highly Sterically Hindered Silanol of the Type (Me 3 Si) 3 CSi(C 6 H 4 Me- p )MeOH and Reaction of the Related Iodide with Iodine Monochloride and Iodine Monobromide

The silanol (Me 3 Si) 3 CSi(C 6 H 4 Me- p )MeOH has been shown to isomerize to (Me 3 Si) 2 CHSi(C 6 H 4 Me- p )(Me)(OSiMe 3 ) when it was kept at room temperature for 10 h in 0.2 M NaOMe/MeOH. Corresponding isomerizations of the above silanol (to give (Me 3 Si) 2 CHSi(C 6 H 4 Me- p ) (Me)(OSiMe 3 )) are complete after 26 h under reflux in pyridine. The reaction involve 1,3-migration from carbon to oxygen within a silanolate ion to give a carbanion, which rapidly acquires a proton from the solvent. Treatment of (Me 3 Si) 3 CSi(C 6 H 4 Me- p )MeOH with MeLi in Et 2 O/THF give, by the same rearrangement, the organolithium reagent (Me 3 Si) 2 CLiSi(C 6 H 4 Me- p )(Me)(OSiMe 3 ) which on treatment with Me 2 SiHCl gives (Me 3 Si) 2 C(SiMe 2 H)Si(C 6 H 4 Me- p )(Me)(OSiMe 3 ) and (Me 3 Si) 2 CHSi(C 6 H 4 Me- p )(Me)(OSiMe 3 ). When the experiment was repeated, but with Me 3 SiCl in place of Me 2 SiHCl, it gives exclusively (Me 3 Si) 2 CHSi(C 6 H 4 Me- p )(Me)(OSiMe 3 ). Treatment of the organolithium reagent (Me 3 Si) 2 CLiSi(C 6 H 4 Me- p )(Me)(OSiMe 3 ) with Mel gives exclusively (Me 3 Si) 2 CMeSi(C 6 H 4 Me- p )(Me)(OSiMe 3 ). The related iodide (Me 3 Si) 3 CSi(C 6 H 4 Me- p )Mel reacts with ICI and IBr to give rearranged (Me 3 Si) 2 C(SiMe 2 X)Si(C 6 H 4 Me- p )Me 2 and unrearranged products (Me 3 Si) 3 CSi(C 6 H 4 Me- p )MeX, (X = Cl, Br) respectively. The rearranged bromide (Me 3 Si) 2 C(SiMe 2 Br)Si(C 6 H 4 Me- p )Me 2 reacts with a range of silver [I] salts AgY (Y = OOCCH 3 , SO 4 2 m ) and Mercury [II] salt HgY 2 (Y = OOCCH 3 , SO 4 2 m ) in glacial CH 3 COOH to give the corresponding species (Me 3 Si) 2 C(SiMe 2 OOCCH 3 )Si(C 6 H 4 Me- p )Me 2 . The reaction of the bromide with AgBF 4 in MeOH or i -PrOH give the corresponding rearranged products (Me 3 Si) 2 C(SiMe 2 Y)Si(C 6 H 4 Me- p )Me 2 (Y = --OMe, --OPr i ).     

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.     

Column preconcentration and electrothermal atomic absorption spectrometric determination of rhodium in some food and standard samples

In the present work, an electrothermal atomic absorption spectrometric method has been developed for the determination of ultra‐trace amounts of rhodium after adsorption of its 2‐(5‐bromo‐2‐pyridylazo)‐5‐diethylaminophenol/tetraphenylborate ion associated complex at the surface of alumina. Several factors affecting the extraction efficiency such as the pH, type of eluent, sample and eluent flow rates, sorption capacity of alumina and sample volume were investigated and optimized. The relative standard deviation for eight measurements of 0.1 ng/mL of rhodium was ±6.3%. In this method, the detection limit was 0.003 ng/mL in the original solution. The sorption capacity of alumina and the linear range for Rh(III) were evaluated as 0.8 mg/g and 0.015–0.45 ng/mL in the original solution, respectively. The proposed method was successfully applied for the extraction and determination of rhodium content in some food and standard samples with high recovery values.     

Density and viscosity of 1-butyl-3-methylimidazolium nitrate with ethanol, 1-propanol, or 1-butanol at several temperatures

Densities and viscosities of 1-butyl-3-methylimidazolium nitrate [Bmim][NO₃], and its binaries with alcohol (ethanol, 1-propanol, or 1-butanol) were measured at different temperatures. The densities and viscosities of pure ionic liquid were correlated successfully by empirical equations. The Vogel–Fulcher–Tammann equations can fit the experimental data of viscosities for pure IL. Excess molar volume and viscosity deviations were calculated for the binaries. The excess molar volumes have negative deviations from the ideal solution.     

C-20 ketone reduction of hydrocortisone by rice field microalga <Emphasis Type="Italic">Chlorella vulgaris</Emphasis> MCCS 013

A unicellular microalga, Chlorella vulgaris, was isolated from rice field and applied in the biotransformation experiment of hydrocortisone (1). This strain has not been previously tested for hydrocortisone bioconversion. Fermentation was carried out in BG-11 medium supplemented with 0.05% substrate at 25°C for 14 days incubation. The products obtained were chromatographically purified followed by their characterization using spectroscopic methods. 11β,17α,20β,21-Tetrahydroxypregn-4-en-3-one (2), 11β,17β-dihydroxyandrost-4-en-3-one (3), and 11β-hydroxyandrost-4-ene-3,17-dione (4) were the main bioproducts in the hydrocortisone bioconversion. Bioreaction characteristics observed were 20-ketone reduction for accumulation of compound 2 and side chain degradation of the substrate to prepare compounds 3 and 4. Time course study showed the accumulation of the product 2 from the second day of the fermentation and 3 as well as 4 from the third day. All the metabolites reached their maximum concentration in seven days. Microalgal 18S rRNA gene was also amplified by PCR. PCR products were sequenced to confirm their authenticity as 18S rRNA gene of microalgae. The result of PCR blasted with other sequenced microalgae in NCBI showed 100% homology to the 18S small subunit rRNA of six strains of Chlorella vulgaris.     

Structure–retardation factor relationship of natural amino acids in two different mobile phases of RP-TLC

Abstract

Separation of amino acids (AAs) and their simple and inexpensive determination/identification is an interesting topic in biological and protein science, different food industries, and drug factories. Also, the presentation of the chromatographic behavior of compounds in a predictive model can be effective to estimate the structural/chemical properties of analyte and mobile phases. In this work for the first time, retardation factor (R_F) of 42 AAs in reversed-phase thin layer chromatography (RP-TLC) was modeled. Acetonitrile-sodium azide solution and 1,2 dioxane-sodium azide solution were two mobile phases which have been studied in this work. Results showed that the values of R_F are correlated with the structural properties of AAs and these properties had some similarities and differences in two noted mobile phases. For the TLC data in two mobile phases, five parametric linear models were suggested (R²_train = 0.93 and 0.97; R²_test = 0.93 and 0.99). The models were also evaluated with different statistical approaches. It was shown that increasing the sum of geometrical distances between N and O in AAs causes decreasing their R_F in RP-TLC using both mobile phases. Other structural effects of AAs on their separation in the desired RP-TLC system were also discussed.