Highly efficient Friedel–Crafts-type benzylation via benzyl cations generated in multiple spacer-molecule separated ion-pairs
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2004/OB/B312664A
Reference47 articles.
1. Aromatic Substitution. X.1 The AlCl3·CH3NO2-Catalyzed Benzylation of Benzene and n-Alkylbenzenes with Benzyl Chloride in Nitromethane Solution
2. Friedel-Crafts isomerization. XV. Aluminum chloride catalyzed isomerization of (methylphenyl)phenylmethanes
3. Aromatic substitution. XXVII. Friedel-Crafts benzylation of toluene and benzene with substituted benzyl chlorides. Substituent effects in the electrophilic substituting agent affecting the nature of the transition state as reflected by substrate and positional selectivity
4. Aromatic substitution. XXVIII. Mechanism of electrophilic aromatic substitutions
5. Aromatic substitution. XXX. Friedel-Crafts benzylation of benzene and toluene with benzyl and substituted benzyl halides
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