944796-76-3

Upstream product

• 944796-75-2 (2R,6S,11bR)-9,10-dimethoxy-2-(methoxycarbonylmethyl)-4-oxo-1,2,3,6,7,11b-hexahydrobenzo[a]quinolizine-6-carboxylic acid 
• 1666-13-3 diphenyl diselenide 
• 909281-78-3 (3S,7R,8aS)-3-(3,4-dimethoxybenzyl)-7-(methoxycarbonylmethyl)-5-oxo-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine 
• 944796-74-1 (2R,6S,11bR)-6-formyl-9,10-dimethoxy-2-(methoxycarbonylmethyl)-4-oxo-1,2,3,6,7,11b-hexahydrobenzo[a]quinolizine 
• 909281-81-8 (2R,6S,11bR)-6-(hydroxymethyl)-9,10-dimethoxy-2-(methoxycarbonylmethyl)-4-oxo-1,2,3,6,7,11b-hexahydrobenzo[a]quinolizine 
• 80582-39-4 (2S)-2-amino-3-(3,4-dimethoxyphenyl)-1-propanol 
• 430461-02-2 dimethyl 3-(2-oxoethyl)pentan-1,5-dioate 

Relevant academic research and scientific papers

Straightforward methodology for the enantioselective synthesis of benzo[a]- and indolo[2,3-a]quinolizidines

(Chemical Equation Presented) An enantioselective two-step route to substituted benzo[a]- and indolo[2,3-a]quinolizidines has been developed. It consists of (i) a stereoselective cyclocondensation of a racemic or prochiral δ-oxo(di)ester with either (S)-(

Complementary routes for the stereoselective synthesis of functionalized benzoquinolizidine targets

We report new and complementary routes for the highly stereoselective construction of functionalized benzoquinolizidine targets from readily available, non-racemic chiral templates. The methods developed allow us to predetermine relative product stereoche