1289142-83-1

Upstream product

• 1176887-94-7 N-((Z)-4-methyl-1-oxo-1-phenylpent-2-en-3-yl)benzamide 
• 3160-32-5 (1E)-4-methyl-1-phenylpent-1-en-3-one 
• 93-97-0 benzoic acid anhydride 
• 305837-96-1 (E)-4-methyl-1-phenylpent-1-en-3-amine 

Relevant academic research and scientific papers

A dual-catalysis/anion-binding approach to the kinetic resolution of allylic amines

Chemical equations presented. A dual-catalysis approach enables the small-molecule catalyzed kinetic resolution of allylic amines by acylation. By employing 2 mol % of each 4-(pyrrolidino)pyridine (PPY) and a readily available chiral hydrogen-bonding coca

Asymmetric synthesis of 4H-1,3-oxazines: Enantioselective reductive cyclization of N-acylated β-amino enones with trichlorosilane catalyzed by chiral Lewis bases

N-Acylated β-amino enones reductively cyclize by treatment with trichlorosilane and a chiral Lewis base catalyst to afford optically active 4H-1,3-oxazines, which can be transformed to other chiral compounds without racemization.