846066-94-2

Upstream product

• 530-62-1 1,1'-carbonyldiimidazole 
• 4397-53-9 p-benzyloxybenzaldehyde 
• 95332-25-5 3-(4-Benzyloxy-phenyl)-oxirane-2-carboxylic acid ethyl ester 
• 124-38-9 carbon dioxide 
• 846066-98-6 ethyl 3-azido-3-(4-(benzyloxy)phenyl)-2-hydroxypropanoate 
• 846066-95-3 3-azido-3-(4-benzyloxy-phenyl)-2-ethoxycarbonyloxy-propionic acid ethyl ester 
• 846066-90-8 ethyl 3-ethoxycarboxamido-2-hydroxy-3-(4-benzyloxyphenyl)propanoate 
• 846067-03-6 3-azido-3-(4-benzyloxy-phenyl)-2-phenoxycarbonyloxy-propionic acid ethyl ester 

Downstream Products

• 846066-96-4 ethyl 4-(4-hydroxyphenyl)-2-oxo-1,3-oxazolane-5-carboxylate 

Relevant academic research and scientific papers

A facile Ph3P/CO2 mediated, one-pot synthesis of 2-oxazolidinones from 1, 2-azido alcohols via phosphazene and isocyanate intermediates

A facile, efficient and convenient method has been developed for the one-pot synthesis of 2-oxazolidinones from the corresponding 1, 2-azido alcohols via phosphazene and isocyanate intermediates in presence of Ph 3P/CO2 in toluene.

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.