112213-44-2

Upstream product

• 701-99-5 Phenoxyacetyl chloride 
• 876-30-2 4-methoxymethyloxyaniline 
• 112237-98-6 (3RS,4SR)-4-<3-diphenyl-t-butylsilyloxyprop-1-ynyl>-1-(4-methoxymethoxyphenyl)-3-phenoxyacetamidoazetidin-2-one 

Downstream Products

• 87112-00-3 C₂₈H₂₉N₃O₈Se 
• 87096-45-5 N-{(2R,3S)-1-(4-Methoxymethoxy-phenyl)-2-[3-(2-nitro-phenylselanyl)-propyl]-4-oxo-azetidin-3-yl}-2-phenoxy-acetamide 
• 87096-47-7 (2RS,6RS,7SR)-benzyl 4-methyl-8-oxo-7-phenoxyacetamido-1,3-diazabicyclo<4.2.0>oct-3-ene-2-carboxylate 
• 87096-47-7 (2RS,6SR,7RS)-benzyl 4-methyl-8-oxo-7-phenoxyacetamido-1,3-diazabicyclo<4.2.0>oct-3-ene-2-carboxylate 
• 112213-45-3 (3RS,4SR)-1--3-phenoxyacetamido-4-prop-2-enylazetidin-2-one 
• 87096-48-8 (2RS,6RS,7RS)-4-methyl-8-oxo-7-phenoxyacetamido-1,3-diazabicyclo<4.2.0>oct-3-ene-2-carboxyic acid 
• 133789-15-8 N-((2R,3S)-2-Ethyl-4-oxo-azetidin-3-yl)-2-phenoxy-acetamide 
• 82792-77-6 (3RS,4SR)-3-phenoxyacetamido-4-prop-2-enylazetidin-2-one 
• 87096-44-4 (3RS,4SR)-4-(3-methylsulphonyloxypropyl)-1-(4-methoxymethoxyphenyl)-3-phenoxyacetamidoazetidin-2-one 
• 87096-46-6 (3RS,4SR)-1-(4-methoxymethoxyphenyl)-3-phenoxyacetamido-4-prop-2-enylazetidin-2-one 
• 87096-43-3 (3RS,4SR)-4-(3-hydroxypropyl)-1-(4-methoxymethoxyphenyl)-3-phenoxyacetamidoazetidin-2-one 

Relevant academic research and scientific papers

Synthesis of Novel Fused β-Lactams by Intramolecular 1,3-Dipolar Cycloadditions. Part 9. Preparation of the 7-Oxo-1,3-dizabicycloheptane-2-carboxylate and 8-Oxo-1,3-dizabicyclooctane-2-carboxylate Ring Systems

4-Vinylazetidin-2-one (24) has been converted into 1--4-vinylazetidin-2-one (27) and 1--4-(2-methoxycarbonylvinyl)-azetidin-2-one (43) which on thermolysis in toluene gave (2RS,5RS)-ben

Synthesis of novel fused β-lactams by intramolecular 1,3-dipolar cycloadditions. 6. Phenoxyacetamido iso-azapenem and iso-azacephem carboxylic acids

6-Phenoxyacetamido-7-oxo-1,3-diazabicyclo [3.2.0] hept-3-ene-2-carboxylic acid and 7-phenoxyacetamido-8-oxo-1,3-diazabicyclo [4.2.0] oct-3-ene-2-carboxylic acid have been prepared and shown to be devoid of antibacterial activity