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    STUDIA CHEMIA - Issue no. 4(II) / 2009  
         
  Article:   SYNTHESIS OF A DIMERIC G-2 MELAMINE DENDRIMER. FIRST USE OF A MASKED PIPERIDONE MOTIF IN DENDRITIC CHEMISTRY.

Authors:  FLAVIA POPA, OANA MOLDOVAN, MARIA IUSCO, PEDRO LAMEIRAS, CARMEN BATIU, YVAN RAMONDENCB, MIRCEA DARABANTU. 		 
       
         
  Abstract:  Using iterative aminations of cyanuric chloride, we account the concise synthesis of a dimeric melamine based G-2 dendrimer having 1,4-dioxa-8-azaspiro[4.5]decane (piperidone ethyleneketal) in tandem with 2-amino-2-hydroxymethylbutanol (“ethylserinol”) as peripheral groups piperazine and 4,4’-bispiperidine as internal and central linker, respectively.

Keywords: amination, dendrimers, iterative synthesis, 4-piperidone, 4,4’-bispiperidine, serinols.
  
         
     
         
         
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