62677-54-7

Upstream product

• 51310-26-0 1,3-diphenyl-2-methyl-1-H-indene 
• 873-66-5 1-propenylbenzene 
• 90-99-3 diphenylchloromethane 
• 766-90-5 cis-1-phenyl-1-propylene 
• 91-01-0 1,1-Diphenylmethanol 
• 93-54-9 1-Phenyl-1-propanol 
• 60999-93-1 2-benzhydryl-1,3-diphenylpropane-1,3-dione 

Relevant academic research and scientific papers

Direct Synthesis of Indanes via Iron-Catalyzed Dehydrative Coupling/Friedel–Crafts Cyclization of Two Different Alcohols

We report herein a novel iron-catalyzed cascade dehydrative coupling/Friedel–Crafts cyclization of two different alcohols, providing a variety of indanes, which are ubiquitous substructures found in natural products, pharmaceuticals, and functional materi

An efficient and general iron-catalyzed C-C bond activation with 1,3-dicarbonyl units as a leaving groups

(Chemical Equation Presented) With our compliments: The 1,3-dicarbonyl unit has been shown to be a new and useful leaving group for iron-catalyzed bond cleavage (see scheme). This new strategy can complement the traditional Friedel-Crafts reaction and was applied in the synthesis of indene derivatives.

Electrochemical Reduction of Activated Carbon-Carbon Double Bonds. Part 2. Mechanism and Stereochemistry of the Reduction of Self-protonating Indenes

The reduction at a mercury electrode in dimethylformamide of five variously substituted indenes bearing at least one (acidic) hydrogen at C(1) was carried out, under self-protonation conditions and in the presence of phenol as a proton donor.Reduction occ