136573-95-0

Upstream product

• 133621-67-7 4-Ethyl-1-<1(H)-indol-3-ylacetyl>-3-(1,3-dimethyl-4,5-diphenylimidazolidin-2-yl)-1,4-dihydropyridine 
• 500-22-1 3-pyridinecarboxaldehyde 
• 22751-68-4 (S,S)-N,N'-dimethyl-1,2-diphenylethane-1,2-diamine 
• 50720-05-3 indolyl acetyl chloride 
• 133634-31-8 3-(1,3-Dimethyl-4(S),5(S)-diphenylimidazolidin-2-yl)pyridine 

Downstream Products

• 136573-96-1 (2R,12bS)-2-Ethyl-1,2,6,7,12,12b-hexahydro-indolo[2,3-a]quinolizine-3-carbaldehyde 
• 136591-52-1 (2R,12bS)-3-((4S,5S)-1,3-Dimethyl-4,5-diphenyl-imidazolidin-2-yl)-2-ethyl-1,2,6,7,12,12b-hexahydro-indolo[2,3-a]quinolizine 

Relevant academic research and scientific papers

Preparation and utilization of chiral dihydropyridines. Synthesis of chiral indoloquinolizines and benzoquinolizines

An asymmetric synthesis of 3-formyl-1,4-dihydropyridines is described that entails the addition of organocopper reagents to activated 3- imidazolidinylpyridine, prepared with chiral diamines. The activator can be a chloroformate or an acid chloride. The m

Enantioselective Synthesis of Indoloquinolizidines. Key words: Chiral 1,4-dihydropyridines - chiral symmetrical diamines - chiral indoloquinolizidines.

Asymmetric synthesis of indoloquinolizidine has been accomplished by using acyl pyridinium salt bearing in 3 position a chiral aminal.