87096-35-3

Upstream product

• 85090-82-0 (3RS,4SR)-4-ethynyl-1-(4-methoxymethoxyphenyl)-3-phenoxyacetamidoazetidin-2-one 

Downstream Products

• 87096-39-7 (2R,5S,6S)-4-Methyl-7-oxo-6-(2-phenoxy-acetylamino)-1,3-diaza-bicyclo[3.2.0]hept-3-ene-2-carboxylic acid 
• 87096-36-4 (3RS,4SR)-3-phenoxyacetamido-4-vinylazetidin-2-one 
• 133789-15-8 N-((2R,3S)-2-Ethyl-4-oxo-azetidin-3-yl)-2-phenoxy-acetamide 
• 112213-46-4 (3RS,4SR)-1--3-phenoxyacetamido-4-vinylazetidin-2-one 
• 87096-39-7 (2RS,5RS,6RS)-4-methyl-7-oxo-6-phenoxyacetamido-1,3-diazabicylo<3.2.0>hept-3-ene-2-carboxylic acid 
• 87096-38-6 (32S,2SR,6SR)-1-benzyl 4-methyl-7-oxo-6-phenoxyacetamido-1,3-diazabicylo<3.2.0>hept-3-ene-2-carboxylate 
• 87096-38-6 (2RS,5RS,6RS)-1-benzyl 4-methyl-7-oxo-6-phenoxyacetamido-1,3-diazabicylo<3.2.0>hept-3-ene-2-carboxylate 

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