158523-64-9

Upstream product

• 204378-59-6 (S)-5-Methoxy-hexahydro-oxazolo[3,4-a]pyridin-3-one 
• 87842-81-7 (6S)-1-aza-2,3-didehydro-8-oxabicyclo[4.3.0]nonan-9-one 
• 85235-51-4 methyl (2S)-2,6-bis(methoxycarbonylamino)hexanoate 
• 88817-74-7 (S)-3,4-Dihydro-2H-pyridine-1,2-dicarboxylic acid dimethyl ester 
• 158523-61-6 (5R,8aS)-5-Azido-hexahydro-oxazolo[3,4-a]pyridin-3-one 

Relevant academic research and scientific papers

First synthesis of optically pure α-amino amine as asymmetric amino transfer reagent and its use in asymmetric Mannich reaction

An optically pure α-amino amine was first synthesized from L-lysine utilizing anodic oxidation as a key step, and its usefulness was exemplified by the asymmetric Mannich reaction to give optically active β-amino acid esters.