A method for oxidation of glycerol into glyceric acid is described, which includes a step of treating glycerol with a supported metal catalyst in the presence of oxygen, said catalyst including platinum and a metal element selected from the group comprising tin, molybdenum, bismuth and a mixture thereof.

A process for preparing amides by reacting a primary amine and a primary alcohol in the presence of a Ruthenium complex to generate the amide and molecular hydrogen. Primary amines are directly acylated by equimolar amounts of alcohols to produce amides and molecular hydrogen (the only byproduct) in high yields and high turnover numbers. Also disclosed are processes for hydrogenation of amides to alcohols and amines; hydrogenation of organic carbonates to alcohols; hydrogenation of carbamates or urea derivatives to alcohols and amines; amidation of esters; acylation of alcohols using esters; coupling of alcohols with water and a base to form carboxylic acids; dehydrogenation of beta-amino alcohols to form pyrazines and cyclic dipeptides; and dehydrogenation of secondary alcohols to ketones. These reactions are catalyzed by a Ruthenium complex which is based on a dearomatized PNN-type ligand of formula A1 or precursors thereof of formulae A2 or A3.

A process for preparing amides by reacting a primary amine and a primary alcohol in the presence of a Ruthenium complex to generate the amide and molecular hydrogen. Primary amines are directly acylated by equimolar amounts of alcohols to produce amides and molecular hydrogen (the only byproduct) in high yields and high turnover numbers. Also disclosed are processes for hydrogenation of amides to alcohols and amines; hydrogenation of organic carbonates to alcohols; hydrogenation of carbamates or urea derivatives to alcohols and amines; amidation of esters; acylation of alcohols using esters; coupling of alcohols with water and a base to form carboxylic acids; dehydrogenation of beta-amino alcohols to form pyrazines and cyclic dipeptides; and dehydrogenation of secondary alcohols to ketones. These reactions are catalyzed by a Ruthenium complex which is based on a dearomatized PNN-type ligand of formula A1 or precursors thereof of formulae A2 or A3.

Provided is a method for preparing glycolic acid which comprises oxidizing glycolaldehyde with molecular oxygen in the presence of a solvent and a supported catalyst. Said supported catalyst comprises (i) a noble metal selected from the group consisting of Pt, Pd, Ru and Rh, (ii) Bi and (iii) a support. Advantageously, the supported metallic catalyst is more active than the catalysts used in prior art. Furthermore, the catalyst is more stable at oxygen rich conditions.

Provided is a method for preparing glycolic acid which comprises oxidizing glycolaldehyde with molecular oxygen in the presence of a solvent and a supported catalyst. Said supported catalyst comprises (i) a noble metal selected from the group consisting of Pt, Pd, Ru and Rh, (ii) Bi and (iii) a support. Advantageously, the supported metallic catalyst is more active than the catalysts used in prior art. Furthermore, the catalyst is more stable at oxygen rich conditions.

Provided is a method for preparing glycolic acid which comprises oxidizing glycolaldehyde with molecular oxygen in the presence of a solvent and a supported catalyst. Said supported catalyst comprises (i) a noble metal selected from the group consisting of Pt, Pd, Ru and Rh, (ii) Bi and (iii) a support. Advantageously, the supported metallic catalyst is more active than the catalysts used in prior art. Furthermore, the catalyst is more stable at oxygen rich conditions.

The present invention provides a production method which is capable of stably producing a catalyst that enables a production of methacrylic acid with high selectivity. A method of producing a catalyst used for a production of methacrylic acid includes (i) preparing a slurry A1 containing a heteropolyacid containing at least phosphorus and molybdenum or a salt of the heteropolyacid containing at least phosphorus and molybdenum, (ii) preparing a slurry A2 satisfying the following Formula (I) and Formula (II) using the slurry A1, (iii) mixing the slurry A2 and a raw material liquid B containing a cationic raw material to prepare a slurry C, and (iv) drying the slurry C, α.sub.A2/α.sub.A1≤0.95 (I), 2≤D.sub.A2≤50 (II), wherein, in Formula (I), α.sub.A1 represents a half-value width (μm) of a particle size distribution of the slurry A1, α.sub.A2 represents a half-value width (μm) of a particle size distribution of the slurry A2, and in Formula (II), D.sub.A2 represents a median diameter (μm) of the particle size distribution of the slurry A2.

The present invention provides a production method which is capable of stably producing a catalyst that enables a production of methacrylic acid with high selectivity. A method of producing a catalyst used for a production of methacrylic acid includes (i) preparing a slurry A1 containing a heteropolyacid containing at least phosphorus and molybdenum or a salt of the heteropolyacid containing at least phosphorus and molybdenum, (ii) preparing a slurry A2 satisfying the following Formula (I) and Formula (II) using the slurry A1, (iii) mixing the slurry A2 and a raw material liquid B containing a cationic raw material to prepare a slurry C, and (iv) drying the slurry C, α.sub.A2/α.sub.A1≤0.95 (I), 2≤D.sub.A2≤50 (II), wherein, in Formula (I), α.sub.A1 represents a half-value width (μm) of a particle size distribution of the slurry A1, α.sub.A2 represents a half-value width (μm) of a particle size distribution of the slurry A2, and in Formula (II), D.sub.A2 represents a median diameter (μm) of the particle size distribution of the slurry A2.

The present invention is directed to the intranasal delivery of curcumin adapted so as to target the brain.

The present invention is directed to the intranasal delivery of curcumin adapted so as to target the brain.