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    STUDIA CHEMIA - Issue no. 1 / 2005  
         
  Article:   FIRST SYNTHESIS, ROTAMERISM AND HERBICIDAL EVALUATION OF SUBSTITUTED S-TRIAZINES WITH SERINOLIC FRAGMENTS (I): OPEN-CHAIN STRUCTURES.

Authors:  MONICA PINTEA, MIRCEA DARABANTU, MARIJANA FAZEKAS, PEDRO LAMEIRAS, CAMELIA BERGHIAN, ISABELLE DELHOM, CONSTANTIN BELE, NELLY PLÉ.
 
       
         
  Abstract:  First series of melamines and precursors, starting from commercially C-substituted-2-amino-1,3-propanediols (pharmaceutical chemistry nomenclature as serinols) in reaction with cyanuryl chloride is reported. The diastereomerism generated by the more or less restricted rotation about the Csp2(s-triazine)-N<(serinol) bond in this series is for the first time discussed along with a preliminary herbicidal evaluation of some representative terms.  
         
     
         
         
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