549548-32-5

Upstream product

• 17342-08-4 (S)-Pyroglutaminol 

Downstream Products

• 549548-35-8 (S)-1-[2-(4-Benzyloxy-phenyl)-allyl]-5-(2-methyl-allyl)-pyrrolidin-2-one 
• 549548-38-1 (6S,7R,8aS)-6-(4-Benzyloxy-phenyl)-6,7-dihydroxy-7-methyl-hexahydro-indolizin-3-one 
• 549548-36-9 (S)-1-[2-(4-Benzyloxy-phenyl)-2-oxo-ethyl]-5-(2-oxo-propyl)-pyrrolidin-2-one 
• 549548-37-0 6-(4-benzyloxy-phenyl)-7-methyl-1,5,8,8a-tetrahydro-2H-indolizin-3-one 
• 549548-39-2 (S)-6-(4-Benzyloxy-phenyl)-7-methyl-1,2,3,5,8,8a-hexahydro-indolizine 
• 23506-90-3 4-[(8aS)-7-methyl-1,2,3,5,8,8a-hexahydroindolizin-6-yl]phenol 

Relevant academic research and scientific papers

Enantiospecific synthesis of an indolizidine alkaloid, (+)-ipalbidine

Enantiospecific total synthesis of an indolizidine alkaloid, ipalbidine, was achieved starting from (-)-pyroglutamic acid by employing an intramolecular McMurry coupling reaction with a low-valent titanium, as a key step.