120566-61-2

Upstream product

• 120566-60-1 5-(Phenylmethyl)-3a,6a-dihydro-1-methylpyrrolo<3,4-d>-1,2,3-triazole-4,6(1H,5H)-dione 
• 15329-69-8 N-benzylmaleamic acid 
• 85843-33-0 N-Benzyl-isomaleimid 
• 100-46-9 benzylamine 
• 1631-26-1 1-benzyl-1H-pyrrole-2,5-dione 

Downstream Products

• 135457-91-9 (+/-)-exo-6-Cyano-8-methyl-2,4-dioxo-3-(phenylmethyl)-3,8-diazabicyclo<3.2.1>octane 
• 135457-92-0 (+/-)-endo-6-Cyano-8-methyl-2,4-dioxo-3-(phenylmethyl)-3,8-diazabicyclo<3.2.1>octane 
• 127381-66-2 (1R-exo)-8-Methyl-2,4-dioxo-3-(phenylmethyl)-3,8-diazabicyclo<3.2.1>octane-6-carboxylic acid ethyl ester 
• 120566-64-5 (+/-)-endo-8-Methyl-2,4-dioxo-3-(phenylmethyl)-3,8-diazabicyclo<3.2.1>octane-6-carboxylic acid methyl ester 
• 120566-63-4 (+/-)-exo-8-Methyl-2,4-dioxo-3-(phenylmethyl)-3,8-diazabicyclo<3.2.1>octane-6-carboxylic acid methyl ester 
• 127381-61-7 <3aS<1<1R^*,5R^*,6R^*>,3aα,6α,7aβ>>-Hexahydro-8,8-dimethyl-1-<<8-methyl-2,4-dioxo-3-(phenylmethyl)-3,8-diazabicyclo<3.2.1>oct-6-yl>carbonyl>-3H-3a,6-methano-2,1-benzisothiazole 2,2-dioxide 
• 127470-56-8 <3aS<1<1S^*,5R^*,6R^*>,3aα,6α,7aβ>>-Hexahydro-8,8-dimethyl-1-<<8-methyl-2,4-dioxo-3-(phenylmethyl)-3,8-diazabicyclo<3.2.1>oct-6-yl>carbonyl>-3H-3a,6-methano-2,1-benzisothiazole 2,2-dioxide 
• 135481-27-5 (1R,5S,6S)-3-Benzyl-8-methyl-2,4-dioxo-3,8-diaza-bicyclo[3.2.1]octane-6-carboxylic acid (1S,2R,4R)-1-[(dicyclohexylsulfamoyl)-methyl]-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 135457-93-1 (1S,5R,6S)-3-Benzyl-8-methyl-2,4-dioxo-3,8-diaza-bicyclo[3.2.1]octane-6-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 135457-93-1 (1S,5R,6R)-3-Benzyl-8-methyl-2,4-dioxo-3,8-diaza-bicyclo[3.2.1]octane-6-carboxylic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester 

Relevant academic research and scientific papers

An Approach to the 3,8-Diazabicyclooctane Moiety of Naphthyridinomycin and Quinocarcin via 1,3-Dipolar Cycloaddition of Photochemically Generated Azomethine Ylides.

An attractive strategy for construction of the 3,8-diazabicyclooctane moiety of targets 1 and 2 involving the 1,3-dipolar cycloaddition of photochemical generated azomethine ylides is presented.