Transition Metal Catalysts

For the determination of choline chloride, primary amine, secondary amine, proline, hydroxyproline precipitant., And Cu +, Hg2 + and Cd2 + chromogenic agent and precipitating agents, environmental protection assay.

DescriptionEnhances stereoselectivity in the radical-mediated allylation of oxysuccinate derivatives.When used in conjunction with Resolve-Al AgFOD, provides an effective NMR shift reagent for aromatic compounds, ammonium salts, and sulfonium and

DescriptionEnhances stereoselectivity in the radical-mediated allylation of oxysuccinate derivatives.When used in conjunction with Resolve-Al AgFOD, provides an effective NMR shift reagent for aromatic compounds, ammonium salts, and sulfonium and

DescriptionEnhances stereoselectivity in the radical-mediated allylation of oxysuccinate derivatives.When used in conjunction with Resolve-Al AgFOD, provides an effective NMR shift reagent for aromatic compounds, ammonium salts, and sulfonium and

DescriptionReactant involved in:Synthesis of rare earth metal complexes for separation of lanthanide metalsConformational mobility of substituted 2-methoxychalcones under the action of lanthanide shift reagentsNMR titration on cation-π complexes of

DescriptionReactant involved in:Synthesis of rare earth metal complexes for separation of lanthanide metalsConformational mobility of substituted 2-methoxychalcones under the action of lanthanide shift reagentsNMR titration on cation-π complexes of

ApplicationPrecursor to organorhenium oxides which catalyze olefin oxidation, metathesis and other transformations. Reagents used for dehydrations and rearrangements of allylic alcohols, oximes, and amides: oxidative cyclizations: alkene metathesis:

ApplicationPrecursor to organorhenium oxides which catalyze olefin oxidation, metathesis and other transformations. Reagents used for dehydrations and rearrangements of allylic alcohols, oximes, and amides: oxidative cyclizations: alkene metathesis:

A catalyst for conjugate reduction of cinnamaldehydes followed by cross-coupling with arylboronic acids. Catalyst for the direct conversion of methane to acetic acid.Catalyst for the isomerization of alkenes, the reduction of aromatic rings, the

A catalyst for conjugate reduction of cinnamaldehydes followed by cross-coupling with arylboronic acids. Catalyst for the direct conversion of methane to acetic acid.Catalyst for the isomerization of alkenes, the reduction of aromatic rings, the

A catalyst for conjugate reduction of cinnamaldehydes followed by cross-coupling with arylboronic acids. Catalyst for the direct conversion of methane to acetic acid.Catalyst for the isomerization of alkenes, the reduction of aromatic rings, the

A catalyst for conjugate reduction of cinnamaldehydes followed by cross-coupling with arylboronic acids. Catalyst for the direct conversion of methane to acetic acid.Catalyst for the isomerization of alkenes, the reduction of aromatic rings, the