846066-95-3

Upstream product

• 541-41-3 chloroformic acid ethyl ester 
• 846066-98-6 ethyl 3-azido-3-(4-(benzyloxy)phenyl)-2-hydroxypropanoate 
• 95332-25-5 3-(4-Benzyloxy-phenyl)-oxirane-2-carboxylic acid ethyl ester 

Downstream Products

• 846066-94-2 ethyl 4-(4-benzyloxyphenyl)-2-oxo-1,3-oxazolane-5-carboxylate 
• 846066-96-4 ethyl 4-(4-hydroxyphenyl)-2-oxo-1,3-oxazolane-5-carboxylate 
• 846066-90-8 ethyl 3-ethoxycarboxamido-2-hydroxy-3-(4-benzyloxyphenyl)propanoate 

Relevant academic research and scientific papers

Studies on synthesis and anti-bacterial activity of novel 4-substituted phenyl-2-oxo-1,3-oxazolidine-5-carboxylates

Regioselective opening of glycidic esters with sodium azide gives azido alcohols, which are converted to novel 4-substituted phenyl-2-oxo-1, 3-oxazolidine-5-carboxylates by various methods. These compounds are tested for in vitro anti-bacterial activity against Staphylococcus aureous, E. faecalis and E. faecium.