95191-94-9

Upstream product

• 32338-54-8 1-(tert-butyl)-3-phenyl-1H-indene 
• 108-86-1 bromobenzene 
• 16618-72-7 3-phenyl-1-indanone 
• 50438-04-5 3-tert-butyl-1-indanone 
• 844-39-3 Dimethyl-4,4 diphenyl-1,1 pentene-1 one-3 
• 95191-87-0 3-tert-Butyl-1-phenyl-indan-1-ol 
• 95191-89-2 C₂₆H₂₈N₂O₂S 
• 431949-52-9 C₁₉H₂₂O 
• 61593-14-4 1-(2-bromophenyl)-2,2-dimethyl-propan-1-one 
• 14900-39-1 phenylvinylboronic acid 
• 102921-26-6 (1,2-dibromoethyl)benzene 
• 98-81-7 1-bromovinylbenzene 
• 6630-33-7 ortho-bromobenzaldehyde 
• 61593-04-2 (±)-1-(2'-bromophenyl)-2,2-dimethyl-1-propanol 

Relevant academic research and scientific papers

The intramolecular reaction of acetophenoneN-tosylhydrazone and vinyl: Br?nsted acid-promoted cationic cyclization toward polysubstituted indenes

In the presence of TsNHNH2, a Br?nsted acid-promoted intramolecular cyclization ofo-(1-arylvinyl) acetophenone derivatives was developed, leading to polysubstituted indenes with complexity and diversity in moderate to excellent yields. In sharp contrast with either the radical or carbene involved cyclization of aldehydicN-tosylhydrazone with vinyl, a cationic cyclization pathway was involved, whereN-tosylhydrazone served as an electrophile and alkylation reagent during this transformation.

Efficient synthesis of indenes by FeCl3·6H2O-catalyzed intramolecular Friedel-Crafts reaction of aryl-substituted allylic alcohols

An efficient procedure for the synthesis of substituted indenes through the FeCl3·6H2O-catalyzed intramolecular Friedel-Crafts cyclization of aryl-substituted allylic alcohols has been developed. This method features the easily avail