900797-83-3Relevant academic research and scientific papers
First synthesis, rotamerism and herbicidal evaluation of substituted s-triazines with amino-1,3-dioxane groups
Fazekas, Marijana,Darabantu, Mircea,Pintea, Monica,Lameiras, Pedro,Bele, Constantin,Berghian, Camelia,Ple, Nelly
, p. 151 - 156 (2006)
First pure enantiomeric 5-amino-1,3-dioxane, obtained by total diastereospecific ring closure of (1S,2S)-2-amino-1-(4-ni-trophenyl)-1,3- propanediol ("nitrophenylserinol") reacted with cyanuryl chloride to afford N-substituted amino-s-triazines and melami
Design, iterative synthesis and structure of novel optically active trispiro-dendritic melamines incorporating 'open-chain' versus 'closed-chain' serinolic peripheral units
Moldovan, Oana,Nagy, Iulia,Lameiras, Pedro,Antheaume, Cyril,Sacalis, Carmen,Darabantu, Mircea
, p. 683 - 701 (2015/07/15)
Abstract Starting from commercial C-2-substituted 2-aminopropane-1,3-diols (serinols, 'open-chain' peripheral units) and optically active amino-1,3-dioxanes ('closed-chain' peripheral units) as cycloacetals of (1S,2S)-2-amino-1-(4-nitrophenyl)propane-1,3-
Serinolic amino-s-triazines: Iterative synthesis of N-substituted amino-1,3-dioxane derivatives from l-(p-nitrophenyl)serinols and rotational stereochemistry phenomena
Fazekas, Marijana,Pintea, Monica,Lameiras, Pedro,Lesur, Amandine,Berghian, Camelia,Silaghi-Dumitrescu, Ioan,Plé, Nelly,Darabantu, Mircea
experimental part, p. 2473 - 2494 (2009/04/10)
We report the first iterative and chemioselective approach towards the synthesis of highly elaborated N-substituted 2,4,6-triamino-s-triazines (melamines) and precursors, by amination of cyanuric chloride with anancomeric and enantiomerically pure primary
