56193-96-5

Upstream product

• 56151-98-5 (3S,4S)-(+)-1-(3,4-dimethoxyphenethyl)-3-ethyl-2-oxo-4-piperidineacetic acid ethyl ester 
• 1835-02-5 2-Bromo-1-(3,4-dimethoxyphenyl)ethanone 
• 56151-97-4 (3R,4S)-(-)-1-(3,4-dimethoxyphenethyl)-3-ethyl-2-oxo-4-piperidineacetic acid ethyl ester 
• 474964-21-1 cinchonine 
• 75821-60-2 (3R,4S)-(+)-1-(3,4-dimethoxyphenacyl)-3-ethyl-4-piperidineacetic acid ethyl ester 
• 75821-62-4 (4S)-1-<2-(3,4-dimethoxyphenyl)-2-hydroxyethyl>-3-ethyl-2-oxo-4-piperidineacetic acid ethyl ester 
• 56151-95-2 (3R,4S)-1-<2-(3,4-dimethoxyphenyl)-2-hydroxyethyl>-3-ethyl-4-piperidineacetic acid ethyl ester 
• 56246-53-8 (+)-ethyl cincholoiponate 
• 21372-26-9 trans-5-ethyl-2-oxo-4-piperidineacetic acid ethyl ester 
• 40173-90-8 3,4-dimethoxyphenethyl bromide 
• 56199-04-3 (+/-)-2-(trans-3-ethyl-[4]piperidyl)-ethanol 

Relevant academic research and scientific papers

Quinolizidines-V. A novel synthetic route to Ipecac alkaloids through chemical incorporation of ethyl cincholoiponate derived from the cinchona alkaloid cinchonine

A new synthetic route to (-)-emetine (1) and related Ipecac alkaloids has been exploited in terms of the synthesis of the tricyclic ester (-)-30 from ethyl cincholoiponate [(+)-4], a degradation product of the Cinchona alkaloid cinchonine (7). The steps i