Selective trimethylsilylation of alcohols and phenols with hexamethyldisilazane catalyzed by LaCoO3 perovskite

Selective conversion of alcohols and phenols to tetrahydropyranyl ethers catalyzed with N-chlorosaccharin under mild and solvent-free conditions

An efficient method is described for the mild and rapid tetrahydropyranylation of alcohols and phenols using a catalytic amount of N-chlorosaccharin (1 mol %) and 3, 4-dihydro-2H-pyran under solvent-free condition at room temperature. Benzylic alcohols and phenols containing electron withdrawing or donating groups in various positions of phenyl ring, cinamyl alcohol, primary, ...

Selective conversion of alcohols and phenols to tetrahydropyranyl ethers catalyzed with N-chlorosaccharin under mild and solvent-free conditions

An efficient method is described for the mild and rapid tetrahydropyranylation of alcohols and phenols using a catalytic amount of N-chlorosaccharin (1 mol %) and 3, 4-dihydro-2H-pyran under solvent-free condition at room temperature. Benzylic alcohols and phenols containing electron withdrawing or donating groups in various positions of phenyl ring, cinamyl alcohol, primary, ...

selective conversion of alcohols and phenols to tetrahydropyranyl ethers catalyzed with n-chlorosaccharin under mild and solvent-free conditions

an efficient method is described for the mild and rapid tetrahydropyranylation of alcohols and phenols using a catalytic amount of n-chlorosaccharin (1 mol %) and 3, 4-dihydro-2h-pyran under solvent-free condition at room temperature. benzylic alcohols and phenols containing electron withdrawing or donating groups in various positions of phenyl ring, cinamyl alcohol, primary, secondary, tertiar...

Silylation of Alcohols and Phenols Using HMDS Catalyzed by SiO2-Cl in Solution and Solvent-Free Conditions

Trimethylsilylation of a variety of alcohols and phenols, in the presence of silica chloride, using hexamethyldisilazane (HMDS) in solution and under solvent-free conditions is reported. Trimethylsilyl ethers were formed in excellent yields both for aliphatic alcohols and phenols without having an electron-withdrawing group. In addition, SiO2-Cl can be recovered and reused after drying.

Selective Acylation of Alcohols in the Presence of Phenols

Selective acylation of alcohol has enjoyed great attraction of chemists due to its significance in synthetic organic chemistry especially in protecting group chemistry as reflected by the number of methods that have been developed to effect this transformation. To meet the challenging task of chemoselective transformation of aliphatic alcohols in the presence of phenolic alcohol mainly acidic c...

Ionic conductivity of perovskite LaCoO3 measured by oxygen permeation technique