122409-98-7

Upstream product

• 2835-06-5 phenylglycin 
• 393-52-2 2-Fluorobenzoyl chloride 

Downstream Products

• 122409-89-6 2-(2-fluorophenyl)-4-phenyl-5(4H)-oxazolone 
• 122409-70-5 2-(2-Fluoro-phenyl)-4-phenyl-4-(1-p-tolyl-1H-[1,2,3]triazol-4-ylmethyl)-4H-oxazol-5-one 
• 122409-68-1 2-(2-Fluoro-phenyl)-4-phenyl-2-[1-(3-trifluoromethyl-phenyl)-1H-[1,2,3]triazol-4-ylmethyl]-2H-oxazol-5-one 
• 122409-92-1 4,4'-bi<2-(2-fluorophenyl)-4-phenyl-5(4H)-oxazolone> 
• 122409-69-2 2-(2-Fluoro-phenyl)-4-(5-morpholin-4-yl-1-p-tolyl-1H-[1,2,3]triazol-4-ylmethyl)-4-phenyl-4H-oxazol-5-one 

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