91859-82-4

Upstream product

• 5324-00-5 2,3-diphenyl-1H-indene 
• 54193-71-4 1,2-epoxy-1,2-diphenyl-indan 
• 103192-02-5 2-[2-((E)-2-Methoxy-1-phenyl-vinyl)-phenyl]-1-phenyl-ethanone 
• 67-56-1 methanol 
• 131618-93-4 (E)-o-(2-phenyl-3-methoxy-2-propenyl)benzophenone 
• 131618-94-5 (Z)-o-(2-phenyl-3-methoxy-2-propenyl)benzophenone 
• 131618-97-8 3,7-diphenyl-3-hydroxy-7-methoxy-4,5-benzo-1,2-dioxacycloheptane 
• 131618-96-7 1,3-diphenyl-1-methoxy-3-hydroperoxyisochroman 
• 53067-91-7 2-(2-benzoylphenyl)-1-phenylethan-1-one 

Downstream Products

• 53067-91-7 2-(2-benzoylphenyl)-1-phenylethan-1-one 
• 93645-91-1 2'-(α-hydroxy-benzyl)-bibenzyl-α-ol 
• 93645-85-3 trans-3,4-dihydro-1,3-diphenyl-1H-2-benzopyran 
• 93645-82-0 cis-3,4-dihydro-1,3-diphenyl-1H-2-benzopyran 
• 4746-79-6 1-(2'-benzoylphenyl)-2-phenylethane-1,2-dione 

Relevant academic research and scientific papers

Ozonide compounds with inhibitory activity for urokinase production and angiogenesis

The invention provides a urokinase production inhibitor or angiogenesis inhibitor comprising as an active component an ozonide derivative represented by the formula (1), and method of prevention or therapy using the inhibitor wherein A is an oxygen atom o

Ozonolyses of 1,2-Diphenyl- and 2-Phenylindene

Ozonolyses of 1,2-diphenylindene (7), 2-phenylindene (18), and the structurally related acyclic keto olefins 13, 14, 26, and 32 were conducted in MeOH/CH2Cl2 at -70 and 0 deg C.The structure of the indenes, 7 and 18, and the rection temperature, were foun

Stereochemical effects on the mechanism of the ozonolysis of (E)- and (Z)-o-(2-phenyl-3-methoxy-2-propenyl)benzophenone

The ozonolyses of (E)- and (Z)-o-(2-phenyl-3-methoxy-2-propenyl)benzophenone (6), which should proceed through a common carbonyl oxide intermediate 15, afforded distinctly different reaction product mixtures, suggesting that the substrate stereochemistry

Ozonolysis of Vinyl Ethers. Evidence for Intramolecular Oxygen Transfer from a Carbonyl Oxide Moiety to a Methoxyvinyl Group

Ozonolysis of diene 1 in carbon tetrachloride gave exclusively the keto ester 2, while in methanol the keto olefin 17 was the major product.The behavior of model vinyl ethers 3a,b has revealed that a mechanism involving intramolecular oxygen atom transfer from the carbonyl oxide moiety to a methoxyvinyl group is the most probable for the keto ester formation from diene 1.

THE PHOTOCHEMICAL PREPARATION OF OZONIDES BY ELECTRON-TRANSFER PHOTO-OXYGENATION OF EPOXIDES

9,10-Dicyanoanthracene (DCA) sensitizes the electron-transfer photo-oxygenation of epoxides in oxygen-saturated acetonitrile to form ozonides.Epoxides with oxidation potentials lower than 2 V vs SCE quench the fluorescence of DCA and are converted to the