36199-58-3

Upstream product

• 3412-44-0 (1E)-1,3-diphenylpropene 
• 36199-57-2 (E)-2,4-diphenylbut-3-enoic Acid 
• 3412-44-0 1,3-diphenylpropene 
• 2294-90-8 1,3-diphenyl-2-propene-1-carboxylic acid 

Downstream Products

• 94848-84-7 1,3-diphenyl-2-propene-1-carbonyl azide 
• 1312184-79-4 (3E)-N-hydroxy-2,4-diphenylbut-3-enamide 
• 1312184-85-2 (3E)-N-(acetoxy)-2,4-phenylbut-3-enamide 
• 104386-86-9 (Z)-3-cyano-l-phenyl-3-phenyl-2-propen-1-one 
• 94848-92-7 benzyl N-(1,3-diphenyl-2-propenyl)carbamate 
• 94848-93-8 C₁₆H₁₃NO 

Relevant academic research and scientific papers

New preparation of (Z)-1-phenyl-3-cyano-2-propen-1-ones

Reaction of γ-phenyl-β,γ-unsaturated hydroxamates with bis(collidine)-bromine(I) hexafluorophosphate led to the formation of cyclic bromo imidates. Reaction of these with triethylamine led to the formation of 3-cyano-2-propen-1-ones with good yields by a

MECHANISMS OF CLASSICAL REARRANGEMENTS IN THE ALLYLIC SERIES. THE CURTIUS REARRANGEMENT

A general method is proposed for the investigation of the rearrangements of unsaturated compounds with the use of stable isotopes.By means of the 13C label it was shown that the Curtius rearrangement of 1,3-diphenyl-2-propene-1-carbonyl azide takes place