246546-97-4

Upstream product

• 2258-42-6 formyl acetic anhydride 
• 246546-95-2 (1S,5S,8aS,8bR)-5-Methylamino-2-oxo-1-((R)-1-trimethylsilanyloxy-ethyl)-1,2,5,6,7,8,8a,8b-octahydro-azeto[2,1-a]isoindole-4-carboxylic acid benzyl ester 
• 35249-73-1 benzyl chlorooxalate 
• 135297-32-4 ((1S,3R)-3-{(2R,3S)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-4-oxo-azetidin-2-yl}-2-oxo-cyclohexyl)-methyl-carbamic acid allyl ester 
• 167950-36-9 benzyl (4S,8S,9R,10S)-1-aza-10-[(R)-1-hydroxyethyl]-11-oxo-4-[(allyloxycarbonyl)(methyl)amino]tricyclo[7.2.0.0^3,8]undec-2-ene-2-carboxylate 
• 167950-27-8 benzyl (4S,8S,9R,10S)-1-aza-10-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-11-oxo-4-[(allyloxycarbonyl)(methyl)amino]tricyclo[7.2.0.0^3,8]undec-2-ene-2-carboxylate 

Downstream Products

• 246546-99-6 benzyl (4S,8S,9R,10S)-1-aza-10-[(R)-1-hydroxyethyl]-11-oxo-4-[(formyl)(methyl)amino]tricyclo[7.2.0.0^3,8]undec-2-ene-2-carboxylate 

Relevant academic research and scientific papers

Synthesis and antibacterial activity of trinems bearing nitrogen derivatives at C(4)

Optimization of the antibacterial activity of 4-amino trinem, obtained through chemical modification of the basicity of the amino group at position 4, has led to the identification of a very interesting compound characterized by a broad spectrum of activi