860469-61-0

Upstream product

• 64471-43-8 (S)-α-cyclopentyl-α-hydroxy-α-phenylacetic acid 
• 90581-53-6 (2S,5S)-2,5-diphenyl-1,3-dioxolan-4-one 
• 611-71-2 (R)-Mandelic Acid 
• 17199-29-0 (S)-Mandelic acid 
• 137-43-9 Cyclopentyl bromide 
• 860644-54-8 (S)-methyl-α-cyclopentyl-α-hydroxyl-α-phenylacetate 
• 230632-95-8 (S)-N-methyl-3-azabicyclo[3,3,1]nonan-9-yl 2'-cyclopentyl-2'-hydroxy-2'-phenylacetate 
• 17341-93-4 2,2,2-Trichloroethyl chloroformate 

Relevant academic research and scientific papers

Optical resolution, stereoselective synthesis, and crystal structure of 9α-(3-azabicyclo[3,3,1]nonanyl)-2′cyclopentyl-2′-hydroxy- 2′-phenylacetate

9α-(3-Azabicyclo[3,3,1 ]nonanyl)-2′-cyclopentyl-2′- hydroxy-2′-phenylacetate (1) was synthesized and its enantiomers were obtained by the optical resolution of racemates with the chiral host N-p-toluenesulfonylglutamic acid. Optical pure 1 was also effect