1401415-25-5Relevant articles and documents
The development of a scalable, chemoselective nitro reduction
Gallagher, William P.,Marlatt, Mark,Livingston, Robert,Kiau, Susanne,Muslehiddinoglu, Jale
supporting information, p. 1665 - 1668 (2013/02/23)
We have demonstrated a scalable chemoselective reduction of a nitro functional group in the presence of an aryl imine using (NH4) 2S/EtOH or hydrogenation (Sponge Nickel) to afford the corresponding amino-imines in moderate to excellent yields. Other reducible groups such as aryl halides, styryl olefins, and ether linkages survived as well.