57164-14-4

Upstream product

• 13638-71-6 9-oxo-1,5-diphenyl-3,7-diaza-bicyclo[3.3.1]nonane-3,7-dicarboxylic acid diethyl ester 
• 50-00-0 formaldehyd 
• 631-61-8 ammonium acetate 
• 102-04-5 1,3-Diphenylpropanone 
• 19066-35-4 5,7-diphenyl-1,3-diaza-adamantan-6-one 
• 1053242-62-8 C₂₇H₂₈N₂O₅ 
• 19066-35-4 5,7-diphenyl-1,3-diazatricyclo[3.3.1.1^3,7]decan-6-one 

Downstream Products

• 13638-66-9 1,5-diphenyl-3,7-bis(p-tolylsulphonyl)-3,7-diazabicyclo<3.3.1>nonan-9-one 
• 14930-85-9 5,7-diphenyl-1,3-diaza-2-thia-tricyclo[3.3.1.1^3,7]decan-6-one 2-oxide 
• 1604777-44-7 2-chloro-5,7-diphenyl-1,3-diaza-2-phospha-tricyclo[3.3.1.1^3,7]decane-6-one 2-oxide 
• 1604777-55-0 sodium 6-oxo-5,7-diphenyl-1,3-diaza-2-phospha-tricyclo[3.3.1.1^3,7]decan-2-olate 2-oxide 
• 17130-73-3 2-benzo[1,3]dioxol-5-yl-5,7-diphenyl-1,3-diaza-adamantan-6-one 
• 79168-89-1 3,7-diacetyl-1,5-diphenyl-3,7-diaza-bicyclo[3.3.1]nonan-9-one 
• 19066-35-4 5,7-diphenyl-1,3-diaza-adamantan-6-one 
• 103566-81-0 3,7-bis-(2-dimethylamino-ethyl)-1,5-diphenyl-3,7-diaza-bicyclo[3.3.1]nonan-9-ol 
• 115000-34-5 3,7-bis-(N,N-dimethyl-glycyl)-1,5-diphenyl-3,7-diaza-bicyclo[3.3.1]nonan-9-one 
• 3576-75-8 5,7-diphenyl-1,3-diaza-adamantan-6-ol 
• 102889-39-4 3,7-bis-chloroacetyl-1,5-diphenyl-3,7-diaza-bicyclo[3.3.1]nonan-9-one 
• 113862-18-3 3,7-diethyl-1,5-diphenyl-3,7-diaza-bicyclo[3.3.1]nonan-9-ol 

Relevant academic research and scientific papers

Anti-neoplastic activity of 1,3-diaza-2-functionalized-adamantan-6-one compounds against melanoma cells

Four series of 1,3-diaza-2-functionalized-adamantan-6-one derivatives, bearing at the 2 position SO, SO2, POCl and PO2H functional groups, were synthesized via a key quadruple Mannich reaction, followed by transformation of an aminal functionality into th

Molecular structure of a macrocyclic bispidinone 15,18-diphenyl-4,7,10-trioxa-1,13-diazatricyclo[11.3.3.1 15,18]eicosan-20-one

A crystal structure of the macrocyclic bispidinone 6 reveals a chair-boat conformation and a variable temperature 1H NMR study demonstrates that in solution this configuration is in a degenerate equilibrium.

Conformational Control in the 3,7-Diazabicyclononane System

The twin-chair or boat-chair conformation of 3,7-diazabicyclononanes can be selected by forming N,N'-derivatives in which the N atoms have planar or pyramidal bonding patterns, respectively, e.g., acyl substituents for the former and arylsulphonyl