748771-91-7

Upstream product

• 2550-26-7 4-Phenyl-2-butanone 
• 501-52-0 3-Phenylpropionic acid 
• 170646-96-5 N-methoxy-N-methyl-3-phenylpropionamide 
• 34914-84-6 1-phenyl-6-hepten-3-one 

Downstream Products

• 220446-49-1 1-phenyl-6-hepten-3-one O-pentafluorobenzoyloxime 
• 220446-46-8 7-phenyl-1-hepten-5-one O-methylsulfonyloxime 
• 646039-19-2 1-phenylhept-6-en-3-one O-methoxyacetyloxime 
• 479350-46-4 C₁₅H₁₉NO₃ 
• 479675-55-3 N-(but-3-enyl)-3-phenylpropanamide 
• 314029-24-8 N-(2-phenylethyl)pent-4-enamide 
• 628691-79-2 3-butenyl phenethyl ketone O-acetyloxime 

Relevant academic research and scientific papers

Copper-catalyzed cyclization and azidation of γ,δ-unsaturated ketone O-benzoyl oximes

An intramolecular imination/azidation sequence has been realized through the tetrakis(acetonitrile)copper(I) hexafluorophophate [Cu(CH3CN)4PF6]-catalyzed reaction of γ,δ-unsaturated ketone O-benzoyl oximes with trimethylsi

Synthesis of Quinolines and 2H-Dihydropyrroles by Nucleophilic Substitution at the Nitrogen Atom of Oxime Derivatives

Isomerization of oxime derivatives was researched in detail to find out the methods for the syn-anti isomerization of O-substituted oximes. Based on these findings were developed simple methods for the preparation of aza-heterocycles from both stereoisomers of oximes. Quinolines were synthesized from β-aryl ketone oximes by treatment with trifluoroacetic anhydride and 4-chloranil. γ,δ-Unsaturated O-methoxyacetyloximes were transformed to 2H-dihydropyrroles by reaction with methoxy-acetic acid.