1394159-51-3

Upstream product

• 140411-20-7 4-iodo-2,6-diisopropylaniline 
• 24544-04-5 2,6-diisopropylbenzenamine 
• 67-56-1 methanol 
• 934008-46-5 N,N'-bis(4-iodo-2,6-diisopropylphenyl)1,4-diazabutadiene 

Downstream Products

• 1394159-53-5 (E,E)-N,N?'-(pyridine-2,6-diylbis-(methanylylidene))bis(4-methoxy-2,6-diisopropylaniline) 
• 1589079-52-6 [1,3-bis(4-methoxy-2,6-diisopropyl)phenyl]imidazolium chloride 
• 1589079-53-7 1,3-bis-(4-methoxy-2,6-diisopropylphenyl)-4,5-dihydroimidazolinium chloride 
• 1619907-28-6 N,N'-bis(4-methoxy-2,6-diisopropylphenylamino)ethane-1,2-diamine 
• 1619907-20-8 N,N'-bis(4-methoxy-2,6-diisopropylphenyl)-1,4-diazabutadiene 

Relevant academic research and scientific papers

A new synthetic route to p -methoxy-2,6-disubstituted anilines and their conversion into n-heterocyclic carbene precursors

The development of new N-heterocyclic carbenes (NHC) is a key feature in this now mainstream research area to access novel chemical properties and reactivity that are essential for the discovery of original applications. Up to now, only a few reliable methods have proven suitable for the preparation of methoxylated anilines to ultimately access methoxylated NHC. We are pleased to report here a straightforward and scalable approach to address this matter. Georg Thieme Verlag Stuttgart. New York.

Iron-catalyzed formation of 2-aminopyridines from diynes and cyanamides

Diynes and cyanamides undergo an iron-catalyzed [2 + 2 + 2] cycloaddition to form highly substituted 2-aminopyridines in an atom-efficient manner that is both high yielding and regioselective. This system was also used to cyclize two terminal alkynes and