91232-22-3

Upstream product

• 2403-27-2 1-(4-bromophenyl)-3-phenyl-2-propen-1-one 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 299456-72-7 1-(4-bromophenyl)ethanone O-acetyl oxime 
• 96155-57-6 1-(4-methoxyphenyl)ethanone O-acetyl oxime 
• 100-52-7 benzaldehyde 
• 59862-55-4 p-bromoacetophenone oxime 
• 2475-92-5 4-methoxyacetophenone oxime 

Relevant academic research and scientific papers

Copper-Catalyzed coupling of oxime acetates with aldehydes: A new strategy for synthesis of pyridines

Copper-catalyzed coupling of oxime acetates with aldehydes offers a new strategy for the synthesis of highly substituted pyridines. This novel method tolerates a wide range of functionality and allows for rapid elaboration of the oxime acetates into a variety of substituted pyridines.

Pyrylium Compounds. XXI. - Structure and Tautomerism of Pseudobases of Unsymmetrically Substituted 2,4,6-Triarylpyrylium Salts

Hydrolytic ring opening of unsymmetrically substituted 2,4,6-triarylpyrylium salts 11 results in a mixture of two tautomeric pseudobases, the penten-1,5-diones 13 and 14.In crystalline state as a rule one of these tautomers markedly predominates, whereas