85174-88-5

Upstream product

• 85174-88-5 cis-2-Oxo-4-phenyloxazolidin-5-carbonsaeure-ethylester 
• 57-13-6 urea 
• 2272-55-1 ethyl trans-3-phenyl-1-oxirane-2-carboxylate 
• 129867-27-2 ethyl 3-azido-2-hydroxy-3-phenylpropanoate 
• 862890-43-5 ethyl (2RS,3SR)-3-tert-butoxycarbonylamino-2-hydroxy-3-phenylpropionate 

Downstream Products

• 85174-88-5 trans-2-Oxo-4-phenyloxazolidin-5-carbonsaeure-ethylester 

Relevant academic research and scientific papers

Stereoselective synthesis of anti-2-oxazolidinones by Ph3P-CCl4-Et3N mediated SN2 cyclization of N-Boc-β-amino alcohols

Ethyl anti-4-substituted phenyl-2-oxo-1,3-oxazolidine-5-carboxylates were synthesized stereoselectively in excellent yields using the Ph3P-CCl4-Et3N system by SN2 cyclization of N-Boc-β-amino alcohols. syn to an

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

Ethyl anti-4-substituted phenyl-2-oxo-1,3-oxazolidine-5-carboxylates have been synthesized stereoselectively from N-Boc-β-amino alcohols by O-tosylation followed by SN2 cyclization. All the compounds prepared are tested for their in vitro anti-

Substituent Dependence in the Synthesis of 2-Oxazolidinones from Phenyloxiranes, 2

In the reaction with urea, the trans configurated glycidic esters 4a-d yield the predominantly new 5-aryl-2-oxooxazolidin-4-carboxylates 5 and 4-aryl-2-oxooxazolidin-5-carboxylates 6. 4,5-cis 5b, 4,5-cis 6b, 4,5-cis 6c, and 4,5-trans 6d have been isolated