98243-24-4

Upstream product

• 98244-29-2 Benzyl-((2S,3S,4R)-2,3,4-tris-benzyloxy-hex-5-enyl)-amine 
• 7558-02-3 potassium bromide 
• 1600-27-7 mercury(II) diacetate 

Downstream Products

• 98244-29-2 Benzyl-((2S,3S,4R)-2,3,4-tris-benzyloxy-hex-5-enyl)-amine 
• 98243-25-5 ((2S,3R,4R,5S)-1-Benzyl-3,4,5-tris-benzyloxy-piperidin-2-yl)-methanol 
• 98243-28-8 ((2R,3R,4R,5R)-1-Benzyl-3,4,5-tris-benzyloxy-piperidin-2-yl)-methanol 
• 118495-38-8 (2R,3R,4S,5R)-1-Benzyl-4,5-bis-benzyloxy-2-methyl-piperidin-3-ol 
• 98243-27-7 ((2S,3R,4R,5R)-1-Benzyl-3,4,5-tris-benzyloxy-piperidin-2-yl)-methanol 
• 118495-41-3 (2S,3R,4S,5R)-1-Benzyl-4,5-bis-benzyloxy-2-methyl-piperidin-3-ol 
• 112019-32-6 N-benzyl-tri-O-benzyl-1,5-dideoxy-1,5-imino-D-galactitol 
• 118495-39-9 (2R,3S,4S,5S)-1-Benzyl-4,5-bis-benzyloxy-2-methyl-piperidin-3-ol 
• 98151-00-9 (2R,3R,4R,5S)-1-benzyl-3,4,5-tri(benzyloxy)-2-methylpiperidine 
• 118495-40-2 N-Benzyl-2,3,4-tri-O-benzyl-1,5-dideoxy-1,5-iminoxylitol 

Relevant academic research and scientific papers

Stereoselective electrophilic cyclizations of δ-aminoalkenes derived from carbohydrates; synthesis of polyhydroxypiperidines

Electrophilic cyclizations of a carbohydrate-derived δ-aminoalkene were studied. lodocyclizations proceeded with moderate steric control to afford the D-gluco-configured piperidine as the major product, More extensive studies with mercuric salts resulted