835923-28-9

Upstream product

• 835923-26-7 methyl (2S,4S)-N-tert-butoxycarbonyl-4-[2'-(6'-methoxypyridyl)]pyrrolidine-2-carboxylate 
• 1499-56-5 (R)-4-hydroxy-L-proline ethyl ester 
• 74844-91-0 1-tert-butyl 2-methyl (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylate 
• 102195-80-2 (S)-1-tert-butyl 2-methyl 4-oxopyrrolidine-1,2-dicarboxylate 
• 835923-25-6 methyl (2S)-N-tert-butoxycarbonyl-4-[2'-(6'-methoxypyridyl)]-2,5-dihydropyrrole-2-carboxylate 
• 462125-00-4 (S)-4-trifluoromethanesulfonyloxy-2,5-dihydro-pyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 

Downstream Products

• 835923-35-8 N-benzyl-5(S)-[2'-(6'-methoxypyridyl)]-2-piperidone 
• 807310-56-1 (+)-N-benzylcytisine 
• 835923-38-1 (3R,5S)-N-benzyl-3-hydroxymethyl-5-[2'-(6'-methoxypyridyl)]piperidine 
• 835923-36-9 N-benzyl-3-ethoxycarbonyl-5(S)-[2'-(6'-methoxypyridyl)]-2-piperidone 

Relevant academic research and scientific papers

Syntheses of (+)-cytisine, (-)-kuraramine, (-)-isokuraramine, and (-)-jussiaeiine A

(Chemical Equation Presented) Total syntheses of (+)-cytisine, (-)-kuraramine, (-)-isokuraramine, and (-)-jussiaeiine A were achieved via a samarium diiodide-promoted reductive deamination reaction, followed by simultaneous recyclization of a proline deri