18949-22-9

Upstream product

• 54398-02-6 1,1-Dichlor-r-2,t-3-dimethyl-2,c-3-diphenylcyclopropan 
• 71-43-2 benzene 
• 29778-21-0 1-isopropyl-2-(2-phenylethynyl)benzene 
• 98-09-9 benzenesulfonyl chloride 
• 5418-21-3 2,3-diphenyl-1-methyl-1H-inden-1-ol 
• 51310-25-9 1-methyl-2,3-diphenylindene 
• 74-88-4 methyl iodide 

Downstream Products

• 96660-95-6 1,1-Dimethyl-3,3-diphenyl-2-indanon 
• 22256-20-8 (Z)-1,1-dimethyl-2,3-diphenylindane 
• 22256-19-5 trans-1,1-dimethyl-3,4-diphenylindan 
• 189230-90-8 2-(2-benzoylphenyl)-2-methyl-1-phenyl-1-propanone 

Relevant academic research and scientific papers

Reusable visible light photoredox catalysts; Catalyzed benzylic C(sp 3)-H functionalization/carbocyclization reactions

The C(sp3)-H functionalization/carbocyclization reaction through the oxidative quenching of visible light photoredox catalysts is established for constructing functionalized 1H-indenes. The process is general for a wide range of benzylic C(sps

Inter- versus Intramolecular Friedel-Crafts Reaction of Phenyl-substituted Dichlorocyclopropanes

Friedel-Crafts reactions of the phenyl-substituted dichlorocyclopropanes 1-9 show different results.Thus, 1 (-> 10, 11), 3 (-> 12), 4(-> 13), 6 (-> 14), 8 (-> 15), and 9 (-> 16) yield indenes by the known intermolecular reaction with benzene.However, 2 (-

Electrochemical Reduction of Activated Carbon-Carbon Double Bonds. 1. Mechanism and Stereochemistry of the Reduction of Phenyl-Substituted Indenes

The reduction at a Hg electrode in DMF of some phenyl-substituted indenes was carried out, with the aim of finding out possible relationships between stereochemistry and mechanism of the reaction.The two-electron two-proton reduction occured exclusively a