740809-95-4

Upstream product

• 80409-67-2 1-(1-naphthyl)-naphthalene-2-carbaldehyde 
• 591-51-5 phenyllithium 
• 741264-28-8 2-[hydroxyl(phenyl)methyl]-1,1'-binaphthyl 
• 740809-94-3 [1,1']binaphthalenyl-2-yl-phenyl-methanone 

Downstream Products

• 740809-97-6 (E)-(+/-)-2-[α-(acetoxyimino)benzyl]-1,1'-binaphthyl 

Relevant academic research and scientific papers

Different recognitions of (E)- and (Z)-1,1′-binaphthyl ketoximes using lipase-catalyzed reactions

Lipase-catalyzed hydrolysis of (E)-2-[α-(acetoxyimino)benzyl]-1, 1′-binaphthyl [(±)-1a] and (Z)-2-[α-(acetoxyimino)benzyl]-1, 1′-binaphthyl [(±)-1b] yielded optically active (E)-2-[α-(hydroxyimino)benzyl]-1,1′-binaphthyl [(S)-2a] and (Z)-2-[α-(hydroxyimino)benzyl]-1,1′-binaphthyl [(R)-2b], respectively, with high enantiomeric excess. Selectivity for the opposite enantiomer of the axial binaphthyl skeleton was shown by (Z)-isomer 1b against (E)-isomer 1a.