401789-18-2

Upstream product

• 75-36-5 acetyl chloride 
• 401789-17-1 (3S,4R)-N-(2-propenyl)-3-(phenylsulfonyl)hept-1-en-4-amine 
• 16212-05-8 (allylsulfonyl)benzene 
• 401789-16-0 (3S,4R)-3-(phenylsulfonyl)hept-1-en-4-amine 
• 401789-15-9 (3S,4R)-3-(phenylsulfonyl)-4-[(S)-(p-tolylsulfinyl)amino]hept-1-ene 

Downstream Products

• 401789-20-6 (2R,3S)-1-acetyl-3-(phenylsulfonyl)-2-propylpiperidine 
• 220073-77-8 (R)-N-acetylconiine 
• 401789-19-3 (2R,3S)-1-acetyl-3-(phenylsulfonyl)-2-propyl-1,2,3,6-tetrahydropyridine 

Relevant academic research and scientific papers

Asymmetric syntheses of N-acetyl-(R)-coniine and N-Boc-(2R,6R)-solenopsin A via ring-closing metathesis

Asymmetric syntheses of piperidine alkaloids N-acetyl-(R)-coniine and (2R,6R)-trans-solenopsin were achieved utilizing stereoselective additions of allylphenylsulfone to chiral alkyl-N-sulfinylimines and ring-closing olefin metathesis.