940899-48-9

Upstream product

• 940899-51-4 N-[(1S,2S)-2-hydroxy-1-methylbut-3-enyl]benzamide 
• 100-39-0 benzyl bromide 
• 7244-67-9 N-benzoyl-L-alanine methyl ester 
• 940899-55-8 C₁₈H₁₉NO₃ 
• 940899-53-6 N-[(1S,2S)-2-benzyloxy-1-methylbut-3-enyl]benzamide 
• 165104-82-5 (2R,3S)-3-benzylamino-2-benzyloxybutan-1-ol 

Downstream Products

• 940899-58-1 C₃₄H₄₆ClNO₄SSi 
• 940899-60-5 (5S,6S)-N-benzyl-5-benzyloxy-2-(tert-butyldimethylsilyloxymethyl)-6-methyl-3-(p-toluenesulfonyl)-2,3-dehydropiperidine 
• 940899-46-7 (5S,6S)-N-benzyl-5-benzyloxy-2-hydroxymethyl-6-methyl-3-(p-toluenesulfonyl)-2,3-dehydropiperidine 
• 940899-62-7 (2S,5S,6S)-N-benzyl-5-benzyloxy-2-hydroxymethyl-6-methyl-3-(p-toluenesulfonyl)piperidine 
• 940899-66-1 (2S,3S,6R)-N-benzyl-3-benzyloxy-6-hydroxymethyl-2-methylpiperidine 
• 940899-70-7 (5S,6S)-N-benzyl-5-benzyloxy-6-methyl-2,3-dehydropiperidine-2-carbaldehyde 
• 940899-44-5 C₂₁H₂₅NO₂ 

Relevant academic research and scientific papers

A highly stereoselective synthesis of (-)-(ent)-julifloridine from the cyclization of an alanine-derived chloroamine with an acetylenic sulfone

(Chemical Equation Presented) The cyclization of γ-chloroamine 11, derived from L-alanine, and acetylenie sulfone 12 afforded the dehydropiperidine 19 via conjugate addition followed by intramolecular alkylation of the corresponding sulfone-stabilized ani