94083-18-8

Upstream product

• 141858-21-1 4-hydroxy-5-<2-(3-hydroxy-1,4-diphenylnaphthyl)>hexan-2-one 
• 20153-17-7 1,4-dimethyl-9,10-diphenylanthracene 1,4-endoperoxide 
• 32314-49-1 1,4-epidioxy-1,4-dimethyl-9,10-diphenyl-1,2,3,4-tetrahydroanthracene 
• 141901-81-7 cis-1,2:3,4-diepoxy-1,4-dimethyl-9,10-diphenyl-1,2,3,4-tetrahydroanthracene 
• 141858-08-4 3,4-epoxy-1,4-dimethyl-9,10-diphenyl-1,2,3,4-tetrahydroanthracen-2-one 
• 141858-19-7 2,5-dimethyl-6,11-diphenyl-4,5-dihydronaphto<2,3-b>oxepin-4-ol 
• 141858-18-6 2,5-dimethyl-6,11-diphenyl-4,5-dihydronaphtho<2,3-b>oxepin-4-one 
• 94083-14-4 2,5-epoxy-2,5-dimethyl-6,11-diphenyl-2,3,4,5-tetrahydronaphtho<2,3-b>oxepine 

Relevant academic research and scientific papers

Photochemical transformations of endoperoxides derived from polycyclic aromatic hydrocarbons, VI. Photo-isomerization of 1,4-endoperoxides and of 1,2,3,4-diepoxides derived from 1,4-dimethylanthracenes

By photolysis at long wavelenghts, 1,4-endoperoxides, 2a,b of 1,4-dimethylanthracenes, 3a,b, isomerized to 1,2;3,4-diepoxides, 1a,b.When irradiated at shorter wavelengths, these compounds led to 3,4-epoxyanthracen-2(1H)-ones, 4a,b, which themselves photo-

Transformations photochimiques d'endoperoxydes derives d'hydrocarbures aromatiques polycycliques IV. Effet de phenyles en peri sur la photo-isomerisation des endoperoxydes-1,4 tetrahydroaromatiques

Photolysis in benzene at long wavelengths of 1,4-epidioxy-1,4-dimethyl-9,10-diphenyl-1,2,3,4-tetrahydroanthracene 1a affords essentially two products: 2,5-epoxy-2,5-dimethyl-6,11-diphenyl-2,3,4,5-tetrahydronaphthooxepine 8a and 5a,8-dimethyl-9-phen