104713-83-9

Upstream product

• 88056-92-2 (-)-2-cyano-6-phenyloxazolopiperidine 
• 74-88-4 methyl iodide 

Downstream Products

• 191470-45-8 (3R,5S)-5-methyl-3-phenyl-2,3,5,6,7,8-hexahydro-oxazolo[3,2-a]pyridine 
• 88154-74-9 (2S,6R)-1-[(1'R)-2'-hydroxy-1'-phenylethyl]-2-methyl-6-propylpiperidine 
• 156873-51-7 (6S)-1-[(1R)-2-hydroxy-1-phenylethyl]-6-methyl-2-piperidone 
• 205526-59-6 (2S,1'R)-N-2'-hydroxy-1'-phenylethyl-2-methylpiperidine 
• 35285-25-7 Solenopsin A 
• 104642-01-5 (3R,5S)-5-Methyl-3-phenyl-8a-undecyl-hexahydro-oxazolo[3,2-a]pyridine 
• 104713-86-2 (2S,6R,1'R)-N-(2-hydroxy-1-phenylethyl)-2-methyl-6-undecylpiperidine 
• 104642-02-6 (2S,6S,1'R)-N-(2-hydroxy-1-phenylethyl)-2-methyl-6-undecylpiperidine 

Relevant academic research and scientific papers

Alkylation studies of a polyhydroxylated-cyano-piperidine scaffold

Hexahydro-3-phenyl-6,7,8-trihydroxy-3R-[3α,5β,6β,7α, 8β,8aβ]-5H-oxazolo[3,2-a]pyridine-5- carbonitrile is endowed with two non equivalent reactive sites: an α-amino nitrile at the C-5 position and an α-amino ether at the C-8a position. Herein, alkylation

Reductive and oxidative transformations of the N-(cyanomethyl)oxazolidine system to expand the chiral pool of piperidines

Two new reactions have been exploited to modify piperidine scaffolds containing the chiral, non-racemic N-(cyanomethyl)oxazolidine system. A Raney nickel mediated decyanation was studied first, followed by an oxidative process using potassium permanganate