924893-94-7

Upstream product

• 140-29-4 phenylacetonitrile 
• 3183-15-1 4-oxo-5-phenylvaleric acid 
• 1380503-44-5 4-(dimethylcarbamoyl)-1-phenyl-2-butyl acetate 
• 21175-42-8 (±)-5-benzyldihydrofuran-2(3H)-one 
• 300-57-2 allylbenzene 
• 924893-87-8 4-hydroxy-N,N-dimethyl-5-phenylpentanamide 
• 108-22-5 Isopropenyl acetate 

Downstream Products

• 1380503-45-6 (S)-4-(dimethylcarbamoyl)-1-phenyl-2-butyl acetate 

Relevant academic research and scientific papers

Lipase-catalyzed kinetic resolution of 2-phenylethanol derivatives and chiral oxa-Pictet-Spengler reaction as the key steps in the synthesis of enantiomerically pure tricyclic amines

A series of 5,6,7,8,9,10-hexahydro-5,9-epoxybenzocycloocten-6-amines have been synthesized and pharmacologically evaluated in receptor binding studies (σ1, σ2, NMDA, κ, and μ receptors). The first key step of the synthesis was a chir

Chemoenzymatic synthesis of enantiomerically pure tricyclic benzomorphan analogues

The key step in the synthesis of enantiomerically pure benzomorphan analogous tricyclic amines 2 is the kinetic resolution of secondary alcohol 7 using the lipase from Pseudomonas fluorescence. The (S)-configured alcohol (S)-7 and the (R)-configured ester