1801-38-3

Upstream product

• 145430-72-4 2-(o-ethenylphenyl)-1,2-diphenylethanone 
• 145430-71-3 ethyl 2-(phenylbenzoylmethyl)cinnamate 
• 50-00-0 formaldehyd 
• 126614-45-7 α-phenyl-α-acetophenone 
• 67-56-1 methanol 

Downstream Products

• 126614-45-7 α-phenyl-α-acetophenone 
• 126614-50-4 6,7-dihydro-6,7-diphenyl-1,6-epoxy-1H-2,4,5-benzotrioxonine 
• 256530-39-9 1,2,4,5-tetrahydro-2,4,5-triphenyl-1,4-epoxy-3,2-benzoxazepin 
• 145430-72-4 2-(o-ethenylphenyl)-1,2-diphenylethanone 
• 145430-71-3 ethyl 2-(phenylbenzoylmethyl)cinnamate 

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

Chemical transformations of solvent-derived ozonolysis products: Improved synthesis of polycyclic 1,2,4,6-tetroxepanes from α-alkoxy α′-hydroperoxy cyclic ethers and aldehydes

α-Alkoxy α′-hydroperoxy cyclic ethers condense with aliphatic aldehydes under acidic conditions to produce the bicyclic 1,2,4,6-tetroxepanes. By X-ray crystallographic analysis, the tetroxepanes 5b and 12b, derived from cyclocondensation of the hydroperoxides 4 and 8 respectively with acetaldehyde, were shown to be exo-isomers.

Cycloaddition between Carbonyl Oxides and Dicarbonyl Compounds: Isolation and Characterization of Novel Polycyclic 1,2,4,6-Tetroxepane Derivatives

Formaldehyde O-oxide reacts with dicarbonyl compounds to produce mono-ozonides formed by conventional cycloadditions to an aldehyde carbonyl group of the substrate, and/or polycyclic 1,2,4,6-tetroxepane derivatives arising from formal cycloadditions involving both carbonyl groups.Similar reactions between the more highly substituted carbonyl oxides, benzaldehyde and octanal O-oxides, and dicarbonyl compounds yielded the corresponding mono-ozonides as the sole isolable cycloaddition products.In certain favorable cases, mono-ozonides could undergo acid-catalysed intramolecular rearrangement to the corresponding 1,2,4,6-tetroxepanes.X-Ray crystallographic analyses of two 1,2,4,6-tetroxepanes, 6a and 13b, are recorded.

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