1316273-91-2

Upstream product

• 2688-91-7 2-(2-nitrophenoxy)biphenyl 
• 2688-92-8 2-Amino-2'-phenyl-diphenylaether 
• 90-43-7 2-Phenylphenol 
• 1493-27-2 ortho-nitrofluorobenzene 
• 1316273-85-4 N-(2-(biphenyl-2-yloxy)phenyl)acetamide 

Downstream Products

• 1316274-01-7 (+)-(S)-11-methyl-4-phenyl-10,11-dihydrodibenzo[b,f][1,4]oxazepine 

Relevant academic research and scientific papers

Synthesis and enantioselective hydrogenation of seven-membered cyclic imines: Substituted dibenzo[b,f][1,4]oxazepines

Highly enantioselective hydrogenation of seven-membered cyclic imines, substituted dibenzo[b,f][1,4]oxazepines, was achieved, with up to 94% ee, by using the [Ir(COD)Cl]2/(S)-Xyl-C3*-TunePhos complex as the catalyst in the presence of morpholine-HCl.