346665-83-6

Upstream product

• 346665-74-5 [4-(1-benzhydryl-azetidin-3-yloxy)-3-fluoro-phenyl]-carbamic acid benzyl ester 
• 346665-72-3 1-benzhydryl-3-(2-fluoro-4-nitro-phenoxy)-azetidine 
• 346665-73-4 4-(1-benzhydryl-azetidin-3-yloxy)-3-fluoro-phenylamine 
• 369-34-6 3,4-difluoronitrobenzene 
• 18621-17-5 1-(diphenylmethyl)-3-hydroxyazetidine 
• 124-63-0 methanesulfonyl chloride 
• 346665-75-6 (R)-3-[4-(1-Benzhydryl-azetidin-3-yloxy)-3-fluoro-phenyl]-5-hydroxymethyl-oxazolidin-2-one 

Downstream Products

• 346665-77-8 N-{3-[4-(1-benzhydryl-azetidin-3-yloxy)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide 
• 346665-78-9 (S)-5-Aminomethyl-3-[4-(1-benzhydryl-azetidin-3-yloxy)-3-fluoro-phenyl]-oxazolidin-2-one 
• 346665-76-7 (R)-5-Azidomethyl-3-[4-(1-benzhydryl-azetidin-3-yloxy)-3-fluoro-phenyl]-oxazolidin-2-one 

Relevant academic research and scientific papers

Novel piperidinyloxy oxazolidinone antimicrobial agents

Oxazolidinone antibacterial agents, where the N-substituted piperazinyl group of eperezolid was replaced with a N-substituted piperidinyloxy moiety, were synthesized and shown to be active against a variety of resistant and susceptible Gram-positive organ