862183-14-0

Upstream product

• 477779-36-5 4-chloro-N²,N⁶-bis[(1S)-1-(hydroxymethyl)-2-methylpropyl]pyridine-2,6-dicarboxamide 
• 477351-94-3 4-bromo-N,N'-bis[(S)-2-hydroxy-1-isopropylethyl]pyridine-2,6-dicarboxamide 
• 477351-95-4 4-bromo-N,N'-bis[(S)-2-chloro-1-isopropylethyl]pyridine-2,6-dicarboxamide 
• 477351-96-5 4-bromo-2,6-bis[(S)-4-isopropyloxazolin-2-yl]pyridine 
• 206647-42-9 4-bromo-2,6-pyridinedicarboxylic acid chloride 
• 162102-81-0 4-bromopyridine-2,6-dicarboxylic acid 
• 142611-35-6 4-chloro-N,N'-bis[(S)-2-chloro-1-isopropylethyl]pyridine-2,6-dicarboxamide 
• 142611-36-7 (4S,4'S)-2,2'-(4-chloropyridine-2,6-diyl)bis(4-isopropyl-4,4-dihydrooxazole) 
• 499-51-4 Chelidamic acid 
• 4722-94-5 4-chloro-2,6-pyridinedicarboxylic acid 
• 71022-75-8 4-chloropyridine-2,6-dicarbonyl dichloride 
• 862183-13-9 4-(4-Bromo-phenoxy)-2,6-bis-((S)-4-isopropyl-4,5-dihydro-oxazol-2-yl)-pyridine 
• 7486-35-3 tri-n-butyl(vinyl)tin 

Relevant academic research and scientific papers

A flexible and versatile strategy for the covalent immobilization of chiral catalysts based on pyridinebis(oxazoline) ligands

Flexible and versatile methods have been developed for the immobilization of chiral pyridinebis(oxazoline) ligands by covalent bonding to a solid support, either by grafting or by polymerization. Different spacers can easily be introduced to modulate the