tetrahydropyranylation of alcohols and phenols, acetylation of aldehydes and n-boc protection of amines are efficiently catalyzed by melamine trisulfonic acid (mtsa). all reactions were performed at room temperature in good to high yields.

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...

Tetrahydropyranylation of alcohols and phenols, acetylation of aldehydes and N-Boc protection of amines are efficiently catalyzed by melamine trisulfonic acid (MTSA). All reactions were performed at room temperature in good to high yields.

the acetylation of various alcohols and phenols was performed successfully using acetic anhydride in the presence of citric acid coated magnetite nanoparticles as catalyst under solvent-free condition and at 45 °c. the catalyst showed high thermal stability and was recovered and reused at least 5 times without any considerable loss of activity. the present process is environmentally benign and ...

1-(Hydroxyacetyl)pyrene has been introduced as a new fluorescent phototrigger for alcohols and phenols. Alcohols and phenols were protected as their corresponding carbonate esters by coupling with fluorescent phototrigger, 1-(hydroxyacetyl)pyrene. Photophysical studies of caged carbonates showed that they all exhibited strong fluorescence properties. Irradiation of the caged carbonates by visib...

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...

n-(diphenylphosphino)triethyl- and tributylammonium salts are introduced as easily prepared, cheap and stable ionic liquids that act as the condensing agent and media for the efficient esterification of acids with alcohols and phenols. this class of ionic liquids is immiscible with the ester products and thus allows simple and easy separation of the desired products from the reaction mixture.

Tetrahydropyranylation of alcohols and phenols, acetylation of aldehydes and N-Boc protection of amines are efficiently catalyzed by melamine trisulfonic acid (MTSA). All reactions were performed at room temperature in good to high yields.

An efficient alumina-supported CuO-catalyzed O-arylation of phenols and aliphatic alcohols with various aryl as well as heteroaryl halides under ligand-free conditions are reported. This protocol provides a variety of diaryl ether and bis-diaryl ether motifs by reacting different aryl/aliphatic halides with differently substituted phenols and saturated alcohols in the presence of a catalytic am...

The acetylation of various alcohols and phenols was performed successfully using acetic anhydride in the presence of Citric acid coated magnetite nanoparticles as catalyst under solvent-free condition and at 45 °C. The catalyst showed high thermal stability and was recovered and reused at least 5 times without any considerable loss of activity. The present process is environmentally benign and ...