Sharif Digital Repository

Different aliphatic and aromatic aldehydes such as isobutyraldehyde, ethanal, n-propanal, n-butanal, n-hexanal, n-octanal, and substituted benzaldehydes were cyclotrimerized into their corresponding 2,4,6-trialkyl-1,3, 5-trioxanes in the presence of commercial bulk zinc oxide at room temperature under neat conditions within a short span of time with high yield and excellent selectivity. Liquid products were formed as a separate phase and were decanted easily, whereas solid products were isolated by simple extraction. Effect of different additives, mol % of catalyst, kind of substrate, and reaction temperature were examined on the progress of cyclotrimerization reaction  

A unique combination of a supported cobalt complex and the first example of supported NHPI in acetic acid gives a surprisingly stable heterogeneous catalytic system for the selective aerobic oxidation of methylaromatics to benzaldehydes at atmospheric pressure. © The Royal Society of Chemistry 2005  

An efficient synthesis of polycyclic indole derivatives is achieved via domino Knoevenagel - hetero-Diels - Alder reaction of O-acrylated salicylaldehyde derivatives with dihydroindole-2-thiones in H2O as solvent. The products are formed in good-to-excellent yields with high regio- and stereoselectivity  

(Chemical Equation Presented) New 2-aryl-4-chloro-3-hydroxy-1H-indole-5,7- dicarbaldehydes were synthesized in three steps from acetophenone derivatives. By oxidation of acetophenones to aryl glyoxals using selenium dioxide and condensation with acetylacetone in the presence of ammonium acetate in water 3-acetyl-5-aryl-4-hydroxy-2-methyl-1H-pyrrols were obtained. 2-Aryl-4-chloro-3-hydroxy-1H-indole-5,7-dicarbaldehydes were synthesized via Vilsmeier-Haack reaction of pyrrole derivatives in moderate yields  

A manganese(II) complex of 2,4,6-tris(2-pyridyl)-1,3,5-triazine (tptz) has been synthesized and characterized by single-crystal X-ray diffraction, elemental analyses, IR, and UV-Vis spectroscopic techniques. Oxidation of alcohols to their corresponding aldehydes and ketones was conducted by this catalyst using oxone (2KHSO5KH-SO4K2SO4) as an oxidant under biphasic reaction conditions (CH2Cl2/H 2O) and tetra-n-butylammonium bromide as phase transfer agent under air at room temperature. Easy preparation, mild reaction conditions, high yields of the products, short reaction times, no further oxidation to the corresponding carboxylic acids, high selectivity and inexpensive reagents make this... 

At room temperature, SO 2- 4/nano-TiO 2 efficiently catalyze the direct Mannich-type reaction of varieties of in situ-generated aldimines using aldehydes and anilines with ketones in a three-component reaction under solvent-free conditions. The reaction proceeds rapidly and affords the correspondingβ-amino ketones in good to high yields with good to excellent stereoselectivity. The catalyst can be recycled for subsequent reactions without any appreciable loss of efficiency  

A series of new ternary zinc(II) complexes [Zn(L1-10)(phen)], where phen is 1,10-phenanthroline and H2L1-10 = tridentate Schiff base ligands derived from the condensation of amino acids (glycine, l-phenylalanine, l-valine, l-alanine, and l-leucine) and salicylaldehyde-5-sulfonates (sodium salicylaldehyde-5-sulfonate and sodium 3-methoxy-salicylaldehyde-5-sulfonate), have been synthesized. The complexes were characterized by elemental analysis, IR, UV-vis, 1H NMR, and 13C NMR spectra. The IR spectra of the complexes showed large differences between νas(COO) and νs(COO), Δν (νas(COO) - νs(COO)) of 191-225 cm-1, indicating a monodentate coordination of the carboxylate group. Spectral data... 

An efficient and simple method for the reduction of aldehydes, ketones and acid chlorides has been accomplished by using NaBH4-solid LiClO 4 in mild conditions at ambient temperature with complete chemoselectivity in reduction of α,β-unsaturated aldehydes and ketones. The reaction is fast with high yield and simple workup. Copyright © Taylor & Francis, Inc  

A simple and sensitive spectrophotometric method is proposed for the simultaneous determination of protocatechuic acid and protocatechuic aldehyde. The method is based on the difference in the kinetic rates of the reactions of analytes with [Ag(NH3)2]+ in the presence of polyvinylpyrrolidone to produce silver nanoparticles. The data obtained were processed by chemometric methods using principal component analysis artificial neural network and partial least squares. Excellent linearity was obtained in the concentration ranges of 1.23-58.56 ?g mL-1 and 0.08-30.39 ?g mL-1 for PAC and PAH, respectively. The limits of detection for PAC and PAH were 0.039 and 0.025 ?g mL-1, respectively  

In this study, 1,4-diazabicy lo[2.2.2] octane (DABCO) tribromide was immobilized on silica support by using 3-chloro propyl trimethoxy silane to obtain a silica-supported DABCO tribromide reagent. The synthesized reagent was characterized with elemental analysis, FT-IR spectroscopy, and thermo-gravimetric analysis (TGA). This reagent has been applied in the conversion of alcohol to corresponding carbonyl compounds. Alcohol oxidation reactions yield in 52-95%, and the reagent may be recycled five times with further bromine treatment  

A one-pot high yielding reductive amination of aldehydes with primary and secondary amines using LiClO4/NaBH4 and LiClO 4/LiAlH4 as reducing agents in diethyl ether is described  

Red mud (RM) which emerges as a by-product from the alumina producing process has been used as an efficient catalyst for one-pot direct synthesis of nitrile compounds from aldehydes and hydroxylamine hydrochloride under microwave irradiation. ©ARKAT USA, Inc  

CuSO4/SiO2 is found to be an efficient and selective medium for the acetalization of aldehydes in the presence of ketones in solvent-free conditions under microwave irradiation. © 2005 Bentham Science Publishers Ltd  

Several aminovinyl phosphonates were prepared in good yield by four-component aminoalkylation of aldehydes with diethyl(trimethylsilyl)amine, triethylphosphite and dimethyl acetylenedicarboxylate mediated by a 5 molar solution of lithium perchlorate in diethyl ether  

In this research, an attempt was made to investigate the potential of nanophotocatalysts for treatment of hazardous wastewater streams. Titanium dioxide nanoparticles (as photocatalyst) were immobilized on a porous and low-density support called "perlite" using a very simple and inexpensive method. TiO2-coated perlite granules were used in a "Floating-bed photoreactor" to study the photocatalytic purification process of a typical wastewater polluted by furfural. The effects of initial concentration, catalyst mass/solution volume ratio, oxidant molar flow, residence time, and light intensity on process removal efficiency, and kinetics of the reactions were studied. SEM analyses showed a... 

Lung cancer (LC) is the leading cause of cancer mortality so, the analysis of exhaled human breath has great significance for early non-invasive diagnosis. Poor selectivity and strong humidity are two bottlenecks for the application of gas sensors to exhaled breath analysis. The development of novel extractive phases for the analysis of exhaled breath by chromatography is therefore a lucrative object. Polyhedral oligomeric silsesquioxanes (POSS) are among the 3D porous materials whose unique properties make them promising coatings for solid-phase microextraction (SPME). Selective enrichment of polar or nonpolar targets depends on the pore size and functional groups on the POSSs. Herein, we... 

Oxidative deprotection of silylethers, acetals and ketals, to their corresponding alcohols, aldehydes and ketones have been achieved using oxygen or air in the presence of cobalt and manganese salts of 4-aminobenzoic acid supported an silica gel as catalysts. Reactions are clean and catalysts can be recovered easily and reused repeatedly  

4-Amino-2-chloroperbenzoic acid supported on silica gel was found to be a versatile and efficient oxidant for the oxidation of aldehydes and ketones to the corresponding carboxylic acids and esters. Copyright © Taylor & Francis, Inc