93503-12-9

Upstream product

• 2243-35-8 2-acetoxyacetophenone 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 532-27-4 1-chloroacetophenone 
• 72335-13-8 4-acetoxy-3-phenyl-2-butenoic acid ethyl ester 

Downstream Products

• 1008-73-7 4-phenyldihydrofuran-2(3H)-one 
• 133056-58-3 (+)-(R,1R,3R)-N-<2-<2-(4,5-Dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxyphenyl>-1-methylethyl>-4-hydroxy-3-phenylbutanamide 
• 133056-58-3 (-)-(S,1R,3S)-N-<2-<2-(4,5-Dimethoxy-2-methyl-1-naphthyl)3,5-dimethoxyphenyl>-1-methylethyl>-4-hydroxy-3-phenylbutanamide 
• 133056-58-3 (+)-(R,1S,3R)-N-<2-<2-(4,5-Dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxyphenyl>-1-methylethyl>-4-hydroxy-3-phenylbutanamide 
• 133056-58-3 (-)-(S,1S,3S)-N-<2-<2-(4,5-Dimethoxy-2-methyl-1-naphthyl)-3,5-dimethoxyphenyl>-1-methylethyl>-4-hydroxy-3-phenylbutanamide 
• 135094-06-3 (-)-(S,S)-4-Hydroxy-3-phenyl-N-(1-phenylethyl)butanamide 
• 135211-20-0 (-)-(R,S)-4-Hydroxy-3-phenyl-N-(1-phenylethyl)butanamide 
• 68844-05-3 4-phenyldihydrofuran-2-one 
• 1008-73-7 (R)-4-phenyl-4,5-dihydrofuran-2(3H)-one 

Relevant academic research and scientific papers

Synthetic Approaches to the Naphthyl-isoquinoline Alkaloids. Part 2. The Total Synthesis of (-)-O-Methylancistrocladine and (+)-O-Methylhamatine and their Enantiomers

An asymmetric total synthesis of the naphthyl-isoquinoline alkaloids (-)-O-methylancistrocladine 39 is described; the synthetic method also provides routes to the atropisomer (+)-O-methylhamatine 43 and the enantiomers of these alkaloids.The asymmetric co

Resolved Monophenolic 2-Aminotetralins and 1,2,3,4,4a,5,6,10b-Octahydrobenzoquinolines: Structural and Stereochemical Cosiderations for Centrally Acting Pre- and Postsynaptic Dopamine-Receptor Agonists

A detailed structure-activity relationship is revealed for resolved, centrally acting dopamine (DA) agonists acting on both pre- and postsynaptic DA receptors.The compounds resolved are 5- and 7-hydroxy-2-(di-n-propylamino)tetralin and cis- and trans-7-hy