95999-87-4

Upstream product

• 95999-85-2 8,10-diaza-2-oxabicyclo<4.2.2>decane-7,9-dione 
• 91238-09-4 8,10-bis(p-methoxybenzyl)-8,10-diaza-2-oxabicyclo<4.2.2>decane-7,9-dione 
• 100-39-0 benzyl bromide 
• 83135-85-7 8,10-dibenzyl-2-oxa-8,10-diazabicyclo<4.2.2>decane-7,9-dione 

Downstream Products

• 96000-01-0 8,10-dibenzyl-8,10-diaza-6-hydroxy-1-<2'-methyl-1'-hydroxy-2',3'-(isopropylidenedioxy)propyl>-2-oxabicyclo<4.2.2>decane-7,9-dione 
• 96000-01-0 8,10-dibenzyl-8,10-diaza-6-hydroxy-1-<2'-methyl-1'-hydroxy-2',3'-(isopropylidenedioxy)propyl>-2-oxabicyclo<4.2.2>decane-7,9-dione 
• 95740-13-9 5(E)-(2-carboxyvinyl)-1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)cytosine sodium salt 

Relevant academic research and scientific papers

Synthesis and antimicrobial evaluation of bicyclomycin analogues

The synthesis and antimicrobial evaluation of novel bicyclomycin analogues are described. The series of analogues were prepared from the basic 8,10-diaza-2-oxabicyclo[4.2.2]decane-7,9-dione (8), 7,9-diaza-2-oxabicyclo[3.2.2]nonane-6,8-dione (9), 8,10-diaz

UNUSUAL BRIDGEHEAD HYDROXYLATIONS VIA SELENOXIDES: EVIDENCE FOR BRIDGEHEAD CARBOCATIONS

Treatment of C-6-phenylselenyl bicyclopiperazinediones with H2O2 affords the C-6-peroxy and C-6-hydroxy bicylic piperazinediones and is rationalized on the basis of intermediate bridgehead carbocations.