122409-99-8

Upstream product

• 609-65-4 o-chlorobenzoyl chloride 
• 2835-06-5 phenylglycin 

Downstream Products

• 122409-77-2 2-(2-Chloro-phenyl)-4-[5-morpholin-4-yl-1-(4-nitro-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-4H-oxazol-5-one 
• 122409-74-9 2-(2-Chloro-phenyl)-4-[1-(4-methoxy-phenyl)-5-morpholin-4-yl-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-4H-oxazol-5-one 
• 122409-71-6 2-(2-Chloro-phenyl)-4-[1-(4-fluoro-phenyl)-5-morpholin-4-yl-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-4H-oxazol-5-one 
• 122409-80-7 2-(2-Chloro-phenyl)-4-(5-morpholin-4-yl-1-p-tolyl-1H-[1,2,3]triazol-4-ylmethyl)-4-phenyl-4H-oxazol-5-one 
• 122409-93-2 4,4'-bi<2-(2-chlorophenyl)-4-phenyl-5(4H)-oxazolone> 
• 122409-78-3 2-(2-Chloro-phenyl)-4-[1-(4-nitro-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-4H-oxazol-5-one 
• 122409-79-4 2-(2-Chloro-phenyl)-2-[1-(4-nitro-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-2H-oxazol-5-one 
• 122409-75-0 2-(2-Chloro-phenyl)-4-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-4H-oxazol-5-one 
• 122409-76-1 2-(2-Chloro-phenyl)-2-[1-(4-methoxy-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-2H-oxazol-5-one 
• 122409-72-7 2-(2-Chloro-phenyl)-4-[1-(4-fluoro-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-4H-oxazol-5-one 
• 122409-73-8 2-(2-Chloro-phenyl)-2-[1-(4-fluoro-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-4-phenyl-2H-oxazol-5-one 
• 122409-81-8 2-(2-Chloro-phenyl)-4-phenyl-4-(1-p-tolyl-1H-[1,2,3]triazol-4-ylmethyl)-4H-oxazol-5-one 
• 122409-90-9 2-(2-chlorophenyl)-4-phenyl-5(4H)-oxazolone 

Relevant academic research and scientific papers

Enantioselective iridium catalyzed α-alkylation of azlactones by a tandem asymmetric allylic alkylation/aza-Cope rearrangement

The development of an iridium catalyzed enantioselective α-alkylation of azlactones has been described. The reaction provides rapid access to a wide range of enantio-enriched quaternary carbon center allylated 2,4-diaryloxazol-5(2H)-ones in excellent yiel