Methods and compositions for the catalytic oxidation of pharmaceutically active compounds, and more particularly to ex vivo methods for predicting in vivo metabolism of pharmaceutically active compounds, including predicting in vivo interaction between two or more pharmaceutically active compounds.

A process for preparing 3-[(S)-7-bromo-2-((2-oxo propyl)amino)-5-pyridin-2-yl-3H-1,4,-benzodiazepin-3-yl]propionic acid methyl ester (compound (FK)), at a high conversion rate with good reproducibility by oxidizing 3-[(S)-7-bromo-2-(2-hydroxypropylamino)-5-pyridin-2-yl-3H-benzo[e][1,4]diazepin-3yl]propionic acid methyl ester (compound (EM)), in the presence of an oxidation catalyst is provided by defining the ammonium ion content of the oxidation reaction mixture.

The invention describes phospho-amino pincer-type ligands, metal complexes thereof, and catalytic methods comprising such metal complexes for conversion of carbon dioxide to methanol, conversion of aldehydes into alcohols, conversion of aldehydes in the presence of a trifluoromethylation agent into trifluorinated secondary alcohols, cycloaddition of carbon dioxide to an epoxide to provide cyclic carbonates or preparation of an amide from the combination of an alcohol and an amine.

Catalyst compositions for the conversion of aldehyde compounds and primary alcohol compounds to olefins are disclosed herein. Reactions include oxidative dehydroxymethylation processes and oxidative dehydroformylation methods, which are beneficially conducted in the presence of a sacrificial acceptor of H.sub.2 gas, such as N,N-dimethylacrylamide.

A method of forming TiO.sub.2ZnO nanoparticles coated by a copper (II) complex includes forming a mononuclear copper complex by treating a ligand with Cu.sup.2+ ions; and immobilizing the mononuclear copper complex on TiO.sub.2ZnO nanoparticles to obtain the TiO.sub.2ZnO nanoparticle coated by the copper (II) complex. The TiO.sub.2ZnO nanoparticles coated by a copper (II) complex thus produced have improved catalytic effectiveness and increased efficiency by reducing catalytic reaction time and temperature, particularly in methods of catalyzing oxidation of an alcohol or of catalyzing decarboxylative bromination of an acid.

A highly pure optically active proton pump inhibitor compound can be produced safely and inexpensively in a high yield and enantioselectivity by a method of producing an optically active sulfoxide of Formula 2 or a salt thereof, comprising oxidizing a sulfide of Formula 1 or a salt thereof with hydrogen peroxide using an iron salt in the presence of a chiral ligand of Formula 3; wherein A is CH or N; R.sup.1 is hydrogen atom, an alkyl optionally substituted by halogen(s), or an alkoxy optionally substituted by halogen(s); one to three R.sup.2 may exist, and each of R.sup.2 is independently an alkyl, a dialkylamino, or an alkoxy optionally substituted by halogen(s) or alkoxy(s); each of R.sup.3 is independently hydrogen atom, a halogen, cyano or the like; R.sup.4 is a tertiary alkyl; and * and ** represent respectively R configuration or S configuration.

##STR00001##

A formic acid decomposition catalyst system includes organometallic complexes having formula 1:

##STR00001## wherein: M is a transition metal; E is P, N, or C (as in imidazolium carbene); R.sub.1, R.sub.2 are independently C.sub.1-6 alkyl groups; o is 1, 2, 3, or 4; R.sub.3 are independently hydrogen, C.sub.1-6 alkyl groups, OR.sub.14, NO.sub.2, halogen; R.sub.4, R.sub.5, R.sub.6, R.sub.7, R.sub.8, R.sub.9, R.sub.10, R.sub.11, R.sub.12, R.sub.13, R.sub.15, R.sub.16 are independently hydrogen or C.sub.1-6 alkyl groups; R.sub.14 is a C.sub.1-6 alkyl group; and X.sup. is a negatively charge counter ion.

A method of preparing glycolide, the method including dehydrative oligomerization and catalytic depolymerization. The dehydrative oligomerization includes stepwise heating a glycolic acid aqueous solution from room temperature to a temperature of between 200 and 210 C., and maintaining the temperature at each corresponding temperature stage, to yield an oligoglycolic acid. The catalytic depolymerization includes adding a binary complex catalytic system to the oligoglycolic acid to yield a reactant mixture, stepwise heating the reactant mixture from room temperature to a temperature of between 280 and 285 C., and maintaining the temperature at each corresponding temperature stage.

A catalyst including, as effective ingredient, complex represented by Formula (1) which contains bidentate ligand including aromatic heterocyclic 5-membered ring having 2 or more nitrogen atoms, or represented by Formula (2) which contains bidentate ligand including: aromatic heterocyclic 5-membered ring having 2 or more nitrogen atoms; and 6-membered ring having 1 or more nitrogen atoms, isomer or salt of the complex: ##STR00001##
where M.sup.1 and M.sup.2 denote transition metal such as iridium; X.sup.1 to X.sup.16 each independently denote nitrogen or carbon; R.sup.1 to R.sup.13 denote, for example, hydrogen atom, alkyl group, or hydroxy group, provided that when X.sup.i (where i denotes 13 to 16) is nitrogen, R.sup.i is absent at position corresponding to the nitrogen; L.sup.1 and L.sup.2 denote, for example, an aromatic anionic ligand; Z.sup.1 and Z.sup.2 denote any ligand or are absent; and m and n denote positive integer, 0, or negative integer.

A method of forming TiO.sub.2ZnO nanoparticles coated by a copper (II) complex includes forming a mononuclear copper complex by treating a ligand with Cu.sup.2+ ions; and immobilizing the mononuclear copper complex on TiO.sub.2ZnO nanoparticles to obtain the TiO.sub.2ZnO nanoparticle coated by the copper (II) complex. The TiO.sub.2ZnO nanoparticles coated by a copper (II) complex thus produced have improved catalytic effectiveness and increased efficiency by reducing catalytic reaction time and temperature, particularly in methods of catalyzing oxidation of an alcohol or of catalyzing decarboxylative bromination of an acid.