Catalysts

(R)-(+)-Bornylamine.

Description(R)-(+)-Methylp-tolyl sulfoxide may be used to prepare (R)-(+)-methyl 3,5-dimethoxy-6-[8-oxo-9-(p-tolylsulfinyl) nonyl] benzoate, an intermediate for (R)-lasiodiplodin synthesis. Its anions undergo addition reaction with nitrones to form

Description(R)-(+)-N,N-Dimethyl-1-(1-naphthyl)ethylamine can react with palladium acetate in acetic acid to form cyclopalladated naphthyl adduct.Base for kinetic resolution of alcohols and acyl halides.

DescriptionThis optically active maleimide undergoes radical copolymerization with styrene to yield a ~1:1 copolymer (~98%). Vinyl copolymers with asymmetric main chains can be used as nonlinear optical materials. Dienophile for diastereoselective

DescriptionAcid for the resolution of amines.

(R)-(+)-N-allyl-α-methylbenzylamine.

(R)-(+)-Tetrahydro-3-furylamine p-toluenesulfonate salt.

(R)-(+)-Tetrahydro-3-furylamine p-toluenesulfonate salt.

(R)-(+)-Tetrahydro-3-furylamine p-toluenesulfonate salt.

(R)-(+)-Tetrahydro-3-furylamine p-toluenesulfonate salt.

Description(R)-(+)-β-Citronellol can undergo:Oxidation to form (R)-(+)-citronellal, an antifungal agent and (R)-(+)-citronellic acid.Intermolecular olefin aziridination with 2,2,2-trichloroethoxysulfonamide to form citronellol aziridine for

(R)-(-)-2-Phenylbutyric acid.