417699-65-1

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 417699-64-0 (2S,6S)-4-carboxybenzyl-1,7-ditosyl-2,6-diisopropyl-1,4,7-triazaheptane 
• 62596-65-0 (2S)-2-isopropyl-1-[(4-methylphenyl)sulfonyl]aziridine 
• 2026-48-4 (S)-valinol 
• 131078-72-3 4-methyl-N-((1S)-2-methyl-1-{[((2S)-3-methyl-2-{[(4-methylphenyl)sulfonyl]amino}butyl)amino]methyl}propyl)benzenesulfonamide 
• 784178-01-4 (2S,6S)-4-acetyl-1,7-di-p-toluenesulfonyl-2,6-di(1-methylethyl)-1,4,7-triazaheptane 
• 784178-04-7 (2S,6S)-4-acetyl-2,6-di(1-methylethyl)-1,7-di-p-toluenesulfonyl-1,4,7-triazacyclononane 

Downstream Products

• 784178-09-2 1,3-di[(3S,8S)-3,8-di(methylethyl)-4,7-di-p-toluenesulfonyl-1,4,7-triazacyclononan-1-ylmethyl]benzene 

Relevant academic research and scientific papers

The synthesis of unsymmetrically N-substituted chiral 1,4,7- triazacyclononanes

A number of chiral unsymmetrically N-substituted 1,4,7-triazacyclononane ligands have been prepared by modular methods. The key step in the synthesis centres on the macrocyclisation of three tertiary amide precursors under standard Richman-Atkins conditio

A concise, modular synthesis of chiral peraza-macrocycles using chiral aziridines

(equation presented) Novel chiral peraza-macrocycles were synthesized from chiral aziridines as a common building block. Efficient syntheses of chiral [26]-N6, [12]-N4, [9]-N3, and [14]-N4 systems were accomplis