150222-15-4

Upstream product

• 150222-14-3 (2S,3R,6S)-6-allyl-2-methyl-N-tosylpiperidin-3-ol 
• 65-85-0 benzoic acid 

Downstream Products

• 150222-19-8 ethyl <6-(2'S,3'S,6'S)-(3'-benzyloxy-2'-methyl-N-tosyl-piperidine-6'-yl)>-2,4-hexadienoate 
• 150222-20-1 ethyl <6-(2'S,3'S,6'S)-(3'-hydroxy-2'-methyl-N-tosyl-piperidine-6'-yl)>-hexanoate 
• 150222-18-7 (2S,3S,6S)-(3-benzyloxy-2-methyl-N-tosyl-6-piperidinyl)-acetaldehyde 
• 150222-17-6 (2S,3S,6S)-6-allyl-3-benzyloxy-2-methyl-N-tosyl-piperidine 
• 150222-21-2 ethyl <6-(2'S,3'S,6'S)-(3'-hydroxy-2'-methyl-N-tosyl-piperidine-6'-yl)>-hexanoate 
• 150222-16-5 (2S,3S,6S)-6-allyl-3-hydroxy-2-methyl-N-tosyl-piperidine 

Relevant academic research and scientific papers

A New Concise Stereoselective Total Synthesis of (+)-Azimic Acid

A new concise stereoselective total synthesis of (+)-azimic acid, which is the immediate precursor of macrocyclic dilactone azimine, has been achieved in eleven steps from (2S,6S)-6-hydroxy-2-methyl-N-tosyl-Δ4-piperidone-3 (5) with a high overa