An efficient tandem synthesis of alkyl aryl ethers, including valuable building blocks of dialdehyde and dinitro groups under microwave irradiation and solvent free conditions on potassium carbonate as a mild solid base has been developed. A series of alkyl aryl ethers were obtained from alcohols in excellent yields by following the Williamson ether synthesis protocol under practical mild condi...

a general, mild and efficient protocol has been developed for the synthesis of esters and thioesters. the process has been taking place using tetra n-butylammonium iodide (tbai) as a phase-transfer catalyst and in the presence of potassium carbonate (k2co3). a wide range of esters and thioesters was prepared in high yields and suitable times by the treatment of alcohols, phenols and thiols with...

a new synthesis of a-hydroxycarboxylates and 2-hydroxybenzoates based on the reaction of acetonides of a-hydroxycarboxylic acids and 2-hydroxybenzoic acid with sodium alkoxides in the corresponding alcohols as solvent is described. in general, decreasing the steric hindrance of the reactants and increasing the boiling points of alcohols increased the yields and decreased the required time for t...

A new synthesis of a-hydroxycarboxylates and 2-hydroxybenzoates based on the reaction of acetonides of a-hydroxycarboxylic acids and 2-hydroxybenzoic acid with sodium alkoxides in the corresponding alcohols as solvent is described. In general, decreasing the steric hindrance of the reactants and increasing the boiling points of alcohols increased the yiel...

T3P/DMSO is shown to be an effective and mild reagent for the one-pot synthesis of furo[2,3-d]pyrimidine-2,4(1H,3H)-diones from a variety of alcohols. Alcohols are oxidized in situ to aldehydes under mild conditions, which undergo a three-component reaction with N,N'-dimethylbarbituric acid and various isocyanides to afford furo[2,3-d]pyrimidine-2,4(1H,3H)-diones in good yields.

A wound signal originates at the site of injury in lettuce (Lactuca sativa L.) leaf tissue and propagates into adjacent tissue where it induces a number of physiological responses which include increased phenolic metabolism with the de novo synthesis of phenylalanine ammonia lyase (PAL, EC 4.3.1.5), the synthesis and accumulation of soluble phenolic compounds (e.g., chlorogenic acid), and subse...