Chiral Ligands

(R)-(+)-1,1′-Bi(2-naphthol).

(R)-(+)-1,1′-Bi(2-naphthol).

(R)-(+)-1,1′-Bi(2-naphthol).

It is used for the preparation of N-alkylated derivatives and use as chiral auxiliaries.1,1′-Binaphthyl-2,2′-diamine derivatives have been used for asymmetric hydrogenations,1 cyclopropanations,2,3 and formation of chiral lactones.3,4,5.

It is used for the preparation of N-alkylated derivatives and use as chiral auxiliaries.1,1′-Binaphthyl-2,2′-diamine derivatives have been used for asymmetric hydrogenations,1 cyclopropanations,2,3 and formation of chiral lactones.3,4,5.

It is used for the preparation of N-alkylated derivatives and use as chiral auxiliaries.1,1′-Binaphthyl-2,2′-diamine derivatives have been used for asymmetric hydrogenations,1 cyclopropanations,2,3 and formation of chiral lactones.3,4,5.

It is used for the preparation of N-alkylated derivatives and use as chiral auxiliaries.1,1′-Binaphthyl-2,2′-diamine derivatives have been used for asymmetric hydrogenations,1 cyclopropanations,2,3 and formation of chiral lactones.3,4,5.

It is used for the preparation of N-alkylated derivatives and use as chiral auxiliaries.1,1′-Binaphthyl-2,2′-diamine derivatives have been used for asymmetric hydrogenations,1 cyclopropanations,2,3 and formation of chiral lactones.3,4,5.

It is used for the preparation of N-alkylated derivatives and use as chiral auxiliaries.1,1′-Binaphthyl-2,2′-diamine derivatives have been used for asymmetric hydrogenations,1 cyclopropanations,2,3 and formation of chiral lactones.3,4,5.

(R)-(+)-1,1,2-Triphenyl-1,2-ethanediol 2-acetate.

(R)-(+)-1,1,2-Triphenyl-1,2-ethanediol 2-acetate.

(R)-(+)-1-(2,4,6-Triisopropylphenyl)ethanol.