728944-08-9

Upstream product

• 167170-14-1 (5R,8aS)-5-(2-Oxo-propyl)-hexahydro-oxazolo[3,4-a]pyridin-3-one 
• 167170-13-0 (S)-3-((E)-3-Oxo-but-1-enyl)-4-(3-phenylselanyl-propyl)-oxazolidin-2-one 
• 167170-11-8 N-(benzyloxycarbonyl)-5-bromonorvaline methyl ester 
• 167170-12-9 (S)-4-(3-Phenylselanyl-propyl)-oxazolidin-2-one 
• 167170-16-3 (2S,6S)-2-Phenylselanylmethyl-6-propyl-piperidine 
• 167170-15-2 (5S,8aS)-5-Propyl-hexahydro-oxazolo[3,4-a]pyridin-3-one 
• 115141-89-4 (4S)-3-(benzyloxycarbonyl)-4-(3-hydroxypropyl)-1,3-oxazolidin-5-one 
• 23632-67-9 (S)-3-[3-(benzyloxycarbonyl)-5-oxooxazolidin-4-yl]propanoic acid 
• 501-53-1 benzyl chloroformate 
• 65266-41-3 (2R,6S)-2-methyl-6-propylpiperidine 

Relevant academic research and scientific papers

Syntheses of (+)- and (-)-dihydropinidine and (+)- and (-)- epidihydropinidine by using yeast reduction of methyl (2-oxocyclohexyl)acetate

(+) and (-)-Dihydropinidine and (+)- and (-)-epidihydropinidine were synthesized from hydroxy esters 1 and 2 which had been prepared by yeast reduction of methyl (2-oxocyclohexyl)acetate. The enantiomeric excess at the C-1 positions of 1 and 2 were both d

Azacycle Synthesis via Radical Cyclization of β-Aminoacrylates.

(Pyrrolidine)- and (piperidine)acetates are efficiently synthesized via radical cyclization of β-aminoacrylates.