Transition Metal Catalysts

Used to oxidize an allylic methylene group in a synthesis of α,β-unsaturated lactones from D-glucose using Grubbs-catalyzed ring-closing metathesis. A stable versatile oxidizing agent for mild and selective oxidation of alcohols.Usually used to

Used to oxidize an allylic methylene group in a synthesis of α,β-unsaturated lactones from D-glucose using Grubbs-catalyzed ring-closing metathesis. A stable versatile oxidizing agent for mild and selective oxidation of alcohols.Usually used to

Used to oxidize an allylic methylene group in a synthesis of α,β-unsaturated lactones from D-glucose using Grubbs-catalyzed ring-closing metathesis. A stable versatile oxidizing agent for mild and selective oxidation of alcohols.Usually used to

Used to oxidize an allylic methylene group in a synthesis of α,β-unsaturated lactones from D-glucose using Grubbs-catalyzed ring-closing metathesis. A stable versatile oxidizing agent for mild and selective oxidation of alcohols.Usually used to

Oxidizing agent for conversion of primary alcohols to aldehydes and ketones acetals to esters and didehydroketones to enones in the presence of tert-butyl hydroperoxide.

Oxidizing agent for conversion of primary alcohols to aldehydes and ketones acetals to esters and didehydroketones to enones in the presence of tert-butyl hydroperoxide.

Oxidizing agent for conversion of primary alcohols to aldehydes and ketones acetals to esters and didehydroketones to enones in the presence of tert-butyl hydroperoxide.

Pyridinium fluorochromate.

Pyridinium fluorochromate.

Pyridinium fluorochromate.

Pyridinium fluorochromate.

DescriptionQPhos Pd G3 is a third generation (G3) Buchwald precatalyst. It is air, moisture and thermally-stable and is highly soluble in a wide range of common organic solvents. It has long life in solutions. Qphos Pd G3 is an excellent reagent for