1414965-72-2

Upstream product

• 60819-40-1 2,4-dichloro-6-(1-hydroxy-2-(hydroxymethyl)but-2-ylamino)-s-triazine 
• 110-85-0 piperazine 
• 1414965-68-6 2-chloro-6-{[1-hydroxy-2-(hydroxymethyl)but-2-yl]amino}-4-{[(4S,5S)-4-(4-nitrophenyl)-1,3-dioxan-5-yl]amino}-s-triazine 
• 161970-50-9 cis-5(S)-amino-4(S)-(p-nitrophenyl)-1,3-dioxane 
• 115-70-8 2-ethyl-2-amino-propane-1,3-diol 

Relevant academic research and scientific papers

Design, iterative synthesis and structure of novel optically active trispiro-dendritic melamines incorporating 'open-chain' versus 'closed-chain' serinolic peripheral units

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-

New serinolic amino-s-triazines by chemoselective amination of cyanuric chloride and their (pro)diastereomerism in restricted rotational phenomena

The highly chemoselective preparation of new elaborated N-unsymmetrically substituted chlorodiamino-s-triazines and melamines, seen as building-blocks for iterative synthesis, is reported. It consisted of amination of cyanuric chloride with commercial C-2