346664-40-2

Upstream product

• 108-24-7 acetic anhydride 
• 369-34-6 3,4-difluoronitrobenzene 
• 109384-19-2 t-butyl 4-hydroxy piperidine-1-carboxylate 
• 250371-88-1 1-[N-(t-butoxycarbonyl)piperidinyl-4-oxy]-2-fluoro-4-nitrobenzene 
• 250372-00-0 4-[1-(t-butoxycarbonyl)piperidin-4-yloxy]-3-fluoroaniline 
• 250372-89-5 tert-butyl 4-[2-fluoro-4-((5R)-5-{[(methylsulfonyl)oxy]methyl}-2-oxo-1,3-oxazolidin-3-yl)phenoxy]piperidine-1-carboxylate 
• 250373-24-1 4-[4-(5-azidomethyl-2-oxo-oxazolidin-3-yl)-2-fluoro-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester 
• 250372-19-1 2-fluoro-1-{N-(t-butoxycarbonyl)piperidinyl-4-oxy}-4-(benzyloxycarbonylamino)benzene 
• 250372-38-4 (R)-[3-[3-fluoro-4-{N-(t-butoxycarbonyl)piperidinyl-4-oxy}phenyl]-2-oxo-5-oxazolidinyl]-methanol 

Relevant academic research and scientific papers

OXAZOLIDINONE DERIVATIVES AS ANTIMICROBIALS

The present invention relates to substituted phenyl oxazolidinones and processes for preparing thereof. This invention also relates to pharmaceutical compositions comprising compounds of the present invention. Such compounds can be useful antimicrobial ag

Novel piperidinyloxy oxazolidinone antibacterial agents. Diversification of the N-substituent

Oxazolidinone antibacterial agents, where the morpholino group of linezolid was replaced with an N-substituted piperidinyloxy moiety, were synthesized and shown to be active against a variety of resistant and susceptible Gram-positive organisms. The funct