61964-82-7

Upstream product

• 88852-05-5 methyl cis-1-(2,4-Dimethoxybenzyl)-3-amino-4-oxoazetidine-2-carboxylate 
• 701-99-5 Phenoxyacetyl chloride 
• 20781-20-8 2,4-Dimethoxybenzylamine 

Downstream Products

• 82493-41-2 (2S,3R)-1-(2,4-Dimethoxy-benzyl)-3-methoxy-4-oxo-3-(2-phenoxy-acetylamino)-azetidine-2-carboxylic acid methyl ester 
• 82493-46-7 Acetylsulfanyl-[(2S,3R)-2-iodomethyl-3-methoxy-4-oxo-3-(2-phenoxy-acetylamino)-azetidin-1-yl]-acetic acid benzhydryl ester 
• 82493-44-5 Hydroxy-[(2S,3R)-2-iodomethyl-3-methoxy-4-oxo-3-(2-phenoxy-acetylamino)-azetidin-1-yl]-acetic acid benzhydryl ester 
• 82498-74-6 Toluene-4-sulfonic acid (2R,3R)-3-methoxy-4-oxo-3-(2-phenoxy-acetylamino)-azetidin-2-ylmethyl ester 
• 82493-47-8 Acetylsulfanyl-[(2S,3R)-2-iodomethyl-3-methoxy-4-oxo-3-(2-phenoxy-acetylamino)-azetidin-1-yl]-acetic acid 
• 82493-42-3 (2S,3R)-3-Methoxy-4-oxo-3-(2-phenoxy-acetylamino)-azetidine-2-carboxylic acid methyl ester 
• 82493-43-4 N-((2S,3R)-2-Iodomethyl-3-methoxy-4-oxo-azetidin-3-yl)-2-phenoxy-acetamide 
• 82498-73-5 N-((2R,3R)-2-Hydroxymethyl-3-methoxy-4-oxo-azetidin-3-yl)-2-phenoxy-acetamide 

Relevant academic research and scientific papers

Substituted azetidinones

Substituted azetidine intermediates for preparing novel bicyclic β-lactam penicillin analogs which have antibacterial activity are disclosed.

Methods and intermediates for preparing cis-4-oxoazetidine intermediates

The stereospecific cycloaddition of nitrogen containing acetic acid halides or anhydrides with Schiff bases having a carbalkoxy group substituted on the methine carbon atom offers new intermediates and methods for preparing synthetic cephalosporin congeners having antibacterial activity.

8-Oxo-4-thia-1-azabicyclo (4.2.0)-oct-2-ene derivatives

Novel bicyclic β-lactams and intermediates useful in their preparation are disclosed. In particular, 7β-acyl-amino- and 7β-amino-8-oxo-4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acids are prepared. The acylated compounds are antibacterial agents.

Cis-4-oxoazetidine intermediates and methods of preparing them

The stereospecific cycloaddition of nitrogen containing acetic acid halides or anhydrides with Schiff bases having a carbalkoxy group substituted on the methine carbon atom offers new intermediates and methods for preparing synthetic cephalosporin congeners having antibacterial activity.

3-Substituted-6β-(amino- and acylamino)-7-oxo-1,3-diazabicyclo[3.2.0]-h

Novel bicyclic β-lactam penicillin analogs which have antibacterial activity and intermediates for the synthesis thereof are disclosed. In particular, 3-acetyl-7-oxo-6β-phenoxyacetylamino-1,3-diazabicyclo[3.2.0]heptane-2-carboxylic acid and derivatives th