Catalysts

Description(S)-(-)-2-(Dibenzylamino)propionaldehyde can be employed as a building block for the preparation of:Linezolid dipeptide derivatives and 3-oxazolidin-2-one analogs.(2R,3S)-3-Dibenzylamine-1-nitrobutan-2-ol by reacting with

DescriptionUseful in the synthesis of 2-amino-6,7-dihydroxy-1,2,3,4-tetrahydronaphthalene, a potent dopamine agonist. Used in the synthesis of sweetening agents, such asN-trifluoroacetyl-L-aspartic acid α-amides and α-anilides.

DescriptionUseful in catalytic asymmetric sulfoxidation of alkyl aryl sulfides and in the kinetic resolution of alkyl aryl sulfoxides.

(S)-(−)-2-Amino-4-methyl-1,1-diphenyl-1-pentanol.

Description(S)-2-Butyl-CBS-oxazaborolidine is a Corey−Bakshi−Shibata (CBS) reagent commonly used in the enantioselective reduction of ketones.

Description(S)-2-Butyl-CBS-oxazaborolidine is a Corey−Bakshi−Shibata (CBS) reagent commonly used in the enantioselective reduction of ketones.

DescriptionBuilding block for chiraltert-butyl substitutedα-lactams, diols, andα-hydroxyketones.

DescriptionBuilding block for chiraltert-butyl substitutedα-lactams, diols, andα-hydroxyketones.

DescriptionBuilding block for chiraltert-butyl substitutedα-lactams, diols, andα-hydroxyketones.

DescriptionChiral phosphoric acid used for the resolution of amines, amino acids, and amino alcohols.

Description(S)-5,5′,6,6′-Tetramethyl-3,3′-di-tert-butyl-1,1′-biphenyl-2,2′-diol, a biphenyl chiral ligand is used to prepare mono- and bidentate phosphites applicable as catalysts in the hydroformylation of allyl cyanide, heterocyclic olefins, and

Description(S)-5,5′,6,6′-Tetramethyl-3,3′-di-tert-butyl-1,1′-biphenyl-2,2′-diol, a biphenyl chiral ligand is used to prepare mono- and bidentate phosphites applicable as catalysts in the hydroformylation of allyl cyanide, heterocyclic olefins, and