120287-49-2

Upstream product

• 124209-80-9 2-Methyl-5-phenyl-5-phenylamino-1,2-epoxy-4-penten-3-one 
• 29808-41-1 2-Methyl-5-phenyl-1,2-epoxy-4-penten-3-one 
• 622-37-7 Phenyl azide 
• 124209-93-4 4-Bromo-2-methyl-5-phenyl-1,2-epoxy-4-penten-3-one 

Downstream Products

• 120287-52-7 3-Methyl-1,6-diphenyl-4-pyridone 
• 124209-96-7 5-Bromo-3-hydroxy-3-methyl-1,6-diphenyl-1,2,3,4-tetrahydro-4-pyridone 
• 124209-89-8 3-Acetoxy-1,6-diphenyl-3-methyl-1,2,3,4-tetrahydro-4-pyridone 

Relevant academic research and scientific papers

SYNTHESIS OF 1,2,3,4-TETRAHYDRO-4-PYRIDINONES BY HETEROCYCLIZATION OF β-AMINO-β-ARYLACRYLOYLOXIRANES

The heterocyclization of β-alkyl(phenyl)aminocinnamoyloxiranes and their α-bromo derivatives under base-catalysis conditions is a convenient method for the synthesis of 3-hydroxytetrahydro-4-pyridinones.

REACTION OF β-ARYLACRYLOXIRANES WITH PHENYL AZIDE. SYNTHESIS AND CHEMICAL TRANSFORMATIONS OF β-PHENYLAMINO-β-ARYLACRYLYLOXIRANES

The reaction of β-arylacrylyloxiranes with phenyl azide by refluxing in dioxane or toluene leads to β-phenylamino-β-aryl-acrylyloxiranes.Epoxypropionyl- and β-hydroxypropionyltriazoles are also isolated when the reaction is carried out in the dark without