126923-28-2

Downstream Products

• 126923-30-6 (S)-(-)-ethyl-α-hydroxy-α-(4-nitrophenyl)-α-phenyl acetate 
• 145264-96-6 (S)-α-hydroxy-α-(4-aminophenyl)-α-phenylacetic acid 
• 627530-32-9 (R)-1-azabicyclo<2.2.2>-oct-3-yl-(S)-α-hydroxy-α-(4-iodophenyl)-α-phenylacetate 
• 139563-14-7 (S,S)-IQNB 
• 145264-97-7 (S)-α-hydroxy-α-(4-iodophenyl)-α-phenylacetic acid 
• 126828-59-9 (R)-(-)-1-azabicyclo<2.2.2>oct-3-yl-(S)-α-hydroxy-α-(4-nitrophenyl)-α-phenyl acetate 
• 88000-61-7 (R)-(-)-1-azabicyclo<2.2.2>oct-3-yl-(S)-(-)-α-hydroxy-α-(4-aminophenyl)-α-phenyl acetate 

Relevant academic research and scientific papers

Preparation and properties of (R)-(-)-1-azabicyclo[2.2.2]oct-3-yl- (R)-(+)-alpha-hydroxy-alpha-(4-[125I]iodophenyl)-alpha-phenyl acetate and (R)-(-)-1-azabicyclo[2.2.2]oct-3-yl-(S)-(-)-alpha-hydroxy-alpha- (4-[125I]iodophenyl)-alpha-phenyl acetate as pote

rac-4-Nitrobenzilic acid was synthesized and resolved with quinidine and quinine to give the corresponding (R)- and (S)-salts. The resolved diastereomeric salts were converted to (R)- and (S)-4-nitrobenzilic acids and subsequent esterification gave their