78602-32-1

Upstream product

• 77-78-1 dimethyl sulfate 
• 78602-30-9 o-prop-1-enylbenzophenone imine hydrochloride 
• 65273-28-1 o-prop-1-enylmagnesium bromide 
• 100-47-0 benzonitrile 
• 70913-21-2 (E/Z)-1-bromo-2-(prop-1-enyl)benzene 
• 6630-33-7 ortho-bromobenzaldehyde 

Downstream Products

• 1370529-37-5 C₁₆H₁₄O₂ 

Relevant academic research and scientific papers

Photochemical studies on aromatic γ,δ-epoxy ketones: Efficient synthesis of benzocyclobutanones and indanones

Irradiation of terminal aromatic γ,δ-epoxy ketones with a 450 W UV lamp led to Norrish type II cyclization/semi-pinacol rearrangement cascade reaction which formed the benzocyclobutanones containing a full-carbon quaternary center, whereas irradiation of substituted aromatic γ,δ-epoxy ketones led to the indanones through a photochemical epoxy rearrangement and 1,5-biradicals cyclization tandem reaction.

Iminyls. Part 9. Intramolecular Addition of an Iminyl to an Alkene

Phenyl o-styrylphenyl iminyl, generated by oxidation of the corresponding O-carboxymethyloxime with persulphate and by thermolysis of the perester of that acid, cyclises to give a mixture of isoquinoline and 1H-isoindole derivatives.The intermediate radicals have been investigated by e.s.r.