Sharif Digital Repository

Various thioamides, especially thiobenzanilides and thioacetomorpholides, bearing a heterocycle ring were efficiently prepared by a modified Willgerodt-Kindler reaction of quinaldine and α- and γ-picoline with anilines and morpholine in the presence of sulfur, and a catalytic amount of DABCO under microwave irradiation  

Nitriles are efficiently transformed to thiomorpholides via the Willgerodt-Kindler reaction under microwave irradiation in solvent-free conditions  

γ-Alumina is used to catalyze the Cannizzaro reaction in the absence of any base under microwave irradiation in high yields. In the case of terephthalaldehyde the reaction is carried out with high selectivity  

Perchloric acid immobilized on silica gel (SiO2-HClO4) has been utilized as a mild and cheap reagent for onepot preparation of different varieties of flavylium salts via tandem reaction of different acetophenones with Salicylaldehydes under solvent-free conditions. Different reaction conditions such as conventional heating and microwave irradiation have been investigated. The corresponding flavylium salts have been prepared in high yields. The procedure is milder and more convenient than the known procedures  

Hetero-Diels–Alder reactions of [60]fullerene with α,β-unsaturated thio-oxindoles (3a, 3b, 3c), prepared from thio-oxindole 1 and heteroaromatic aldehydes (2a, 2b, 2c), to generate tetrahydrothiopyrano[2,3-b]indole [60]fullerene cycloadducts (5a, 5b, 5c) under thermal or microwave irradiation were described. The yields were improved, and the reaction time was decreased by conducting the reaction under microwave irradiation. © 2016 Wiley Periodicals, Inc  

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  

A solvent-free, solid-supported, and microwave-assisted thio-Claisen rearrangement of S-propargylated thioamides having an activated α-methylene group has been developed. The methodology could be used successfully for the synthesis of tri-substituted thiophenes and sulfur containing triarylamines. The reaction takes place in short time and in good isolated yield. © 2005 Taylor & Francis  

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  

Phenolic compounds and carboxylic acids are methylated with dimethyl carbonate in the presence of a catalytic amount of BF3· OEt2, DBU, or KOH, in good to excellent yields under microwave irradiation and solvent-free conditions  

An AlCl3-ZnCl2 mixture supported on silica gel is found to be a new efficient medium for the Beckmann rearrangement in solvent-free conditions under microwave irradiation. The yields are good to excellent  

Tabas coal sample from Iran was desulfurized with combination of microwave irradiation and peroxyacetic acid washing in a batch reactor. The effect of irradiation time and power, peroxyacetic acid reaction time and temperature and particle size on reduction of sulfur was investigated. For microwaved/acid washed samples, depending on desulfurization conditions, the reduction in pyritic, organic and total sulfur ranged from 26 to 91, 2.6 to 38.4 and 17 to 65%, respectively. Microwave irradiation had positive effect on desulfurization with peroxyacetic acid. For <300 μm size fraction, after irradiation, the reduction enhanced from 49.9 to 86.6% in pyritic sulfur, 23.8 to 35% in organic sulfur... 

The one-pot, three-component condensation of benzil, benzonitrile derivatives and primary amines on the surface of silica gel under solvent-free conditions and microwave irradiation provided tetrasubstituted imidazoles in high yields. © 2003 Elsevier Science Ltd. All rights reserved  

A simple method for the preparation of industrially important alkyl aryl ethers is reported. Several phenolic compounds such as phenols, naphthols, and hydroxy coumarins were O-methylated with trimethyl phosphite or trimethyl phosphate under microwave irradiation and solvent-free condition in almost quantitative yields. Reaction of 2-naphthol with trimethyl phosphate gave mixture of 2-methoxynaphthalene and 1-methyl-2-methoxynaphthalene while the reaction with trimethyl phosphite gave mostly 2-methoxynaphthalene. This method is highly efficient for the methylating of phenolic compounds with very easy experimental procedure and environmental friendly conditions  

Microwave induced Cannizzaro reaction, which was performed in presence of neutral γ-alumina as a polymeric catalyst, was discussed. Cannizzaro reaction was carried out on alumina surface and other unknown products were also obtained. Solvent extraction method was utilized to isolate mild and selective benzyl alcohol and carboxylic acids  

Aryl schiff bases were efficiently reduced to the corresponding secondry amines by triethylammonium formate/formic acid system under microwave irradiation in solvent-free condition  

We report a simple, fast, efficient and benign procedure for solvent-free microwave-assisted one-pot synthesis of symmetrical 4H-pyran-4-ones in the presence of polyphosphoric acid or diphosphorous pentoxide. Various 4H-pyran-4-ones were prepared using this very simple and fast green protocol. ©2007 Sociedade Brasileira de Química  

Iodic acid supported on wet silica gel and K10 clay are used for the efficient oxidation of benzylic alcohols under microwave irradiation and solvent free condition  

Aryl benzylsulfonates undergo so-called pseudo-thia-Fries rearrangement under microwave irradiation. Benzylated phenolic compounds have been obtained with the loss of 'SO2' from the starting materials  

Reaction of aromatic α-bromoketones, sodium azide and aromatic or aliphatic terminal acetylenes in the presence of Cu/Cu(OTf)2following the classical method (aqueous acetonitrile at room temperature) and under microwave irradiation (H2O at 85 °C) leads to 1,4-disubstituted 1,2,3-triazoles as the final products after simple filtration  

A simple, fast and efficient benign procedure has been developed for one-pot synthesis of 2-substituted benzothiazoles in the presence of zirconium(IV) oxide chloride octahydrate (ZrOCl2·8H 2O) and anhydrous copper(II) sulfate. The reaction of 2-aminothiophenol with aldehydes and anhydrides was carried out efficiently in solvent-free conditions with or without microwave irradiation, and adducts were produced in good to excellent yields. © 2006 Wiley Periodicals, Inc