1301743-50-9

Upstream product

• 1301743-49-6 (3R,4S)-4-hydroxy-6-(3-methoxy-3-oxopropyl)-3-(4-methoxyphenyl)-2,3,4,5-tetrahydropyridine-1-oxide 
• 1301743-48-5 (6S,7R)-methyl 6-hydroxy-7-(4-methoxyphenyl)-8-nitro-4-oxooctanoate 
• 1301743-54-3 methyl 3-(2-((2S, 3R)-2-hydroxy-3-(4-methoxyphenyl)-4-nitrobutyl)-1,3-dioxolan-2-yl)propanoate 

Downstream Products

• 23506-90-3 4-[(8aS)-7-methyl-1,2,3,5,8,8a-hexahydroindolizin-6-yl]phenol 
• 1242597-75-6 (6S,8aR)-6-(4-methoxyphenyl)hexahydroindolizin-7(1H)-one 
• 1242597-68-7 (6R,7S,8aS)-octahydro-6-(4-methoxyphenyl)-7-methylindolizin-7-ol 
• 1301743-55-4 (6R,7S,8aS)-hexahydro-7-hydroxy-6-(4-methoxyphenyl)indolizin-3(5H)-one 
• 1301743-53-2 (S)-1,2,8,8a-tetrahydro-7-(3,4-dimethoxyphenyl)-6-(4-methoxyphenyl)indolizin-3(5H)-one 
• 1301743-57-6 (S)-1,2,3,5,8,8a-hexahydro-6-(4-methoxyphenyl)-3-oxoindolizin-7-yl-trifluoromethanesulfonate 
• 1301743-52-1 (6R,8aS)-hexahydro-6-(4-methoxyphenyl)indolizine-3,7-dione 
• 1301743-51-0 (6R,7S,8aS)-octahydro-6-(4-methoxyphenyl)indolizin-7-ol 
• 1242597-79-0 (S)-1,2,3,5,8,8a-hexahydro-7-(3,4-dimethoxyphenyl)-6-(4-methoxyphenyl)indolizine 
• 104069-35-4 (8aS)-6-(4-methoxyphenyl)-7-methyl-1,2,3,5,8,8a-hexahydroindolizine 

Relevant academic research and scientific papers

A simple enantioselective route to functionalized indolizidines: Synthesis of (+)-ipalbidine and (+)-antofine

An efficient route to functionalized indolizidines from an enantiomerically enriched γ-nitro ketone is described. The nitro ketone is obtained by an organocatalytic, enantioselective ketone-nitro alkene Michael addition. Oxidative ring expansion of the ni