Highly electronically deactivated benzylic alcohols, including those with a CF3 group adjacent to the OH-bearing carbon, undergo dehydrative Friedel–Crafts reactions upon exposure to catalytic Brønsted acid in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) solvent. Titration and kinetic experiments support the involvement of higher order solvent/acid clusters in catalysis
We report here a method of direct Friedel–Crafts benzylation of arenes with benzylic alcohols using ...
Dual Brønsted/Lewis acid catalysis involving environmentally benign, readily accessible protic acid ...
2-Furoic acid, aluminum chloride and substituted benzenes give 6-substituted-l-naphthoic acids. For ...
The catalytic activation of alcohols towards dehydrative bond formation in the absence of pre-activa...
This PhD thesis detailed how HFIP in combination with Brønsted and Lewis acids havedemonstrated thei...
Epoxides and primary alcohols are important building blocks for organic synthesis. Efficient strateg...
The development of general and more atom-economical catalytic processes for Friedel–Crafts alkylatio...
International audienceAlcohols and epoxides are arguably ideal electrophiles for the Friedel-Crafts ...
Since its discovery in 1877, the Friedel-Crafts alkylation reaction has been the method of choice to...
After the initial discovery by Friedel and his American associate, James Mason Crafts, that anhydrou...
Alcohols are attractive electrophilic partners for nucleophilic substitution reactions as water is t...
Due to the electron-withdrawing character of fluoroalkyl groups, fluorinated alcohols such as triflu...
We report here a method of direct Friedel–Crafts benzylation of arenes with benzylic alcohols using ...
Dual Brønsted/Lewis acid catalysis involving environmentally benign, readily accessible protic acid ...
2-Furoic acid, aluminum chloride and substituted benzenes give 6-substituted-l-naphthoic acids. For ...
The catalytic activation of alcohols towards dehydrative bond formation in the absence of pre-activa...
This PhD thesis detailed how HFIP in combination with Brønsted and Lewis acids havedemonstrated thei...
Epoxides and primary alcohols are important building blocks for organic synthesis. Efficient strateg...
The development of general and more atom-economical catalytic processes for Friedel–Crafts alkylatio...
International audienceAlcohols and epoxides are arguably ideal electrophiles for the Friedel-Crafts ...
Since its discovery in 1877, the Friedel-Crafts alkylation reaction has been the method of choice to...
After the initial discovery by Friedel and his American associate, James Mason Crafts, that anhydrou...
Alcohols are attractive electrophilic partners for nucleophilic substitution reactions as water is t...
Due to the electron-withdrawing character of fluoroalkyl groups, fluorinated alcohols such as triflu...
We report here a method of direct Friedel–Crafts benzylation of arenes with benzylic alcohols using ...
Dual Brønsted/Lewis acid catalysis involving environmentally benign, readily accessible protic acid ...
2-Furoic acid, aluminum chloride and substituted benzenes give 6-substituted-l-naphthoic acids. For ...