178681-78-2

Upstream product

• 178681-54-4 (R)-2-(m-methoxyphenyl)-2-methylmalonic monoester 
• 178681-55-5 ethyl (S)-(-)-3-hydroxy-2-(m-methoxyphenyl)-2-methylpropionate 
• 178681-56-6 (S)-2-(3-Methoxy-phenyl)-2-methyl-3-oxo-propionic acid ethyl ester 
• 178681-77-1 (S)-3-hydroxy-(m-methoxyphenyl)-2-methylpropionic acid 
• 83026-48-6 diethyl (3-methoxyphenyl)methylpropanedioate 
• 50874-07-2 2-(3-methoxyphenyl)malonic acid diethyl ester 
• 35553-92-5 ETHYL 3-METHOXYPHENYLACETATE 

Downstream Products

• 178681-82-8 (1R,9S)-10-Acetyl-4-methoxy-1-methyl-10-aza-tricyclo[7.2.1.0^2,7]dodeca-2⁽⁷⁾,3,5-trien-8-one 
• 128524-63-0 (+)-8-O-methylaphanorphine 
• 118964-06-0 (-)-aphanorphine 
• 178681-58-8 (R)-2-(3-Methoxy-phenyl)-2-methyl-pentanedioic acid 1-ethyl ester 

Relevant academic research and scientific papers

Asymmetric synthesis of benzylic quaternary carbon center via an enzymatic reaction

(R)-(+)- ((R)-(+)-12) and(S)-(-)-1-formyl-1-methyl-7-methoxy-1,2,3,4-tetrahydronaphthalene((S)-(-)-12) were synthesized based on enantioselective PLE hydrolysis of diethyl 2-(m-methoxyphenyl)-2-methylmalonate. From (R)-(+)-12, (+)-O-Methylaphanorphine (16