Synthesis of Bicyclic Compounds Derived from 1,2,4-Benzotriazines

The synthesis of bicyclic compounds derived from benzo[1,2,4]triazines is described.     

Dipyrromethane as a new organic reagent for the synthesis of gold nanoparticles: preparation and application

Condensation reaction of several ketones with pyrrole in the presence of ferric hydrogen sulfate as a green homogenous acidic catalyst furnished the corresponding pure dipyrromethanes in good yields. Gold nanoparticles were produced through reduction of HAuCl₄ with substituted dipyrromethanes as new reducing agents at room temperature with the exclusion of any capping agent or surfactant. Gold nanoparticles were characterized by transmission electron microscopy, scanning electron microscopy, XRD and UV–visible absorption spectroscopic measurements. It is proposed that in situ formed oxidative products of dipyrromethane, such as polydipyrromethane could serve effectively as a capping agent to preferably adsorb the {111} facets of gold crystals during the reduction process, which leads to the formation of gold nanoparticles.     

Selective monotetrahydropyranylation of symmetrical diols using P_20_5/Si0_2 under solvent-free conditions and their depyranylation

Selective protection of one of the hydroxyl group in 1,n-symmetrical diols is achieved by P_2O_2/SiO_2-catalyzed reaction of the diol with dihydropyran under solvent-free conditions at room temperature.This selective protection is simple and it occurred under economically cheap conditions in high yield.The deprotected diol is simply obtained by refluxing of this compound in methanol using the same catalyst without any byproduct formation or additional purifications.     

Synthesis of imidazo[4,5-<Emphasis Type="Italic">a</Emphasis>]acridones and imidazo[4,5-<Emphasis Type="Italic">a</Emphasis>]acridines as potential antibacterial agents

Abstract  New imidazo[4,5-a]acridone derivatives were synthesized from the rearrangement of 3H-imidazo[4′,5′:3,4]benzo[c]isoxazoles. New imidazo[4,5-a]acridines were obtained from the reaction of imidazo[4,5-a]acridones in boiling POCl₃. All of these compounds exhibited antimicrobial activities comparable to streptomycin as reference drug. Graphical abstract        

Preyssler-type heteropoly acid:A new,mild and efficient catalyst for protection of carbonyl compounds

Preyssler-type heteropoly acid is introduced as a new,mild and efficient catalyst for protection of a variety of carbonyl compounds with 1,3-propane dithiol.     

An Eco‐friendly Three Component Manifold for the Synthesis of α‐Aminophosphonates under Catalyst and Solvent‐free Conditions,X‐ray Characterization and Their Evaluation as Anticancer Agents

A series of α‐aminophosphonates were synthesized through one‐pot condensation of aryl aldehydes, aryl amines and diethyl phosphite in the absence of any catalyst and organic solvents. All the synthesized α‐aminophosphonates were characterized by spectral and elemental analysis and in the case of compound 4j by X‐ray crystallography. Some of these new α‐aminophosphonate derivatives were found to have cytotoxic activity on the cancer cell line DU145 in vitro by the MTT method.     

PPh3-catalyzed Mannich reaction: a facile one-pot synthesis of β-amino carbonyl compounds under solvent-free conditions at room temperature

Research on Chemical Intermediates - PPh3 was used as an efficient catalyst for the one-pot three-component Mannich reactions of acetophenone with different aromatic amines and aromatic aldehydes...