4746-79-6

Upstream product

• 1801-42-9 2,3-diphenyl-1H-inden-1-one 
• 18636-54-9 1,2-diphenyl-1H-indene 
• 53067-91-7 2-(2-benzoylphenyl)-1-phenylethan-1-one 
• 62423-27-2 phenyl-(3-phenyl-isobenzofuran-1-yl)-ketone 
• 171969-52-1 1,3-Diphenyl-isochroman 
• 53133-97-4 1.2c-dihydroxy-1r.2t-diphenyl-indanone-⁽³⁾ 
• 546-67-8 lead(IV) tetraacetate 
• 71-43-2 benzene 
• 67-64-1 acetone 
• 5324-00-5 2,3-diphenyl-1H-indene 
• 24423-97-0 1,2,3-triphenyl-1-propene 
• 221458-86-2 (phenyl)[2-(2-phenylethynyl)phenyl]methanone 
• 91859-82-4 1,4-Diphenyl-4,5-dihydro-1H-1,4-epoxido-benzo[d][1,2]dioxepin 
• 64-19-7 acetic acid 

Downstream Products

• 5471-63-6 1,3-diphenylisobenzofuran 
• 5398-11-8 3-phenylphthalide 
• 60079-98-3 10-phenyl-9-anthracene-ol 
• 39127-30-5 2-butyl-3-phenylisoindolin-1-one 
• 1726-15-4 3-phenyl-2-(phenylmethyl)-2,3-dihydro-1H-isoindol-1-one 
• 85-52-9 2-Benzoylbenzoic acid 
• 65-85-0 benzoic acid 

Relevant academic research and scientific papers

Method for preparing 1,2-dicarbonyl compound by photocatalytic oxidation reaction

The invention discloses a method for preparing a 1,2-dicarbonyl compound by a photocatalytic oxidation reaction. The method includes the following steps: mixing an unsaturated triple bond compound, acoordination catalyst and a solvent to obtain a solution

Iodine/water-mediated oxidation of o-alkynylaroyl compounds and application of the products of oxidation in the synthesis of nitrogen heterocycles

A facile iodine/water-mediated oxidation of the triple bond of o-alkynylaroyl compounds to furnish tricarbonyl compounds is reported. The reaction proceeds through the formation of isochromenol intermediates by the assistance of the neighbouring aroyl gro

Reaction of 1,2,4,5-Tetroxan with Antimony Pentachloride or Liquid Sulphur Dioxide: Heterolytic Fission of Carbon-Oxygen or Oxygen-Oxygen Bonds

The reactions of 11 kinds of tetroxans with antimony pentachloride have been investigated.A mixture of ketone (aldehyde) and ester (carboxylic acid) was obtained, the ratio of which was found to depend on the substituents.In the presence of the catalyst cis-3,6-bis(3-benzoylpropyl)-1,2,4,5-tetroxan rearranges to the trans-isomer.In the reaction of some tetroxans with liquid sulphur dioxide, a mixture of ester and ketone was obtained in a molar ratio of 1:1.Reductive ozonolysis of some alkenes in the presence of 10 mol equiv. of sulphur dioxide in methylene chloride gave the corresponding carbonyl compounds in good yields.