WOS: 000325204200122Since alkyl Lewis acids are Bronsted bases, they give a non-acidic reaction media. In this context, acylation of thiophene is investigated in the presence of EtAlCl2 and non-acidic media. Besides 8 examples of thiophene, one example for pyrrole is synthesized in moderate to high yields (up to 99 %)
The reactivity of thiophene in Diels-Alder reactions is investigated with different maleimide deriva...
A simple and single-step synthesis of 2- and 3-acyl substituted benzothiophenes has been described v...
The Friedel-Crafts acylation of anisole with acetic anhydride could be efficiently catalyzed by sui...
WOS: 000325204200122Since alkyl Lewis acids are Bronsted bases, they give a non-acidic reaction medi...
Heteroaromatic compounds, such as thiophenes, pyrroles and furans, were acylated using zeolite Beta,...
Friedel–Crafts reaction is one of the oldest carbon–carbon bond forming processes and is still an at...
To date, great efforts have been made by different research groups to achieve the goal of making the...
Synthesis of fine chemicals and intermediates by using Friedel–Crafts acylations is an important pro...
Chlorothiophenes react with active aromatic compounds in the presence of AlCl3 under mild conditions...
A new highly efficient catalytic procedure for the Friedel–Crafts acylation of electron rich aromati...
Traditional Friedel-Crafts acylation reactions of aromatics suffer from low regio-selectivity toward...
Indian Institute of Chemical Biology, 4 RajaS. C. Mullick Road, Jadavpur, Calcutta-700 032, India M...
The double Friedel–Crafts acylation of readily accessible biaryls with oxalyl chloride delivers the ...
Herein, a method for thioacetalation using BF3SMe2 is presented. The method allows for convenient an...
This paper reports different examples of Friedel-Crafts acylation of various substrates with dicarbo...
The reactivity of thiophene in Diels-Alder reactions is investigated with different maleimide deriva...
A simple and single-step synthesis of 2- and 3-acyl substituted benzothiophenes has been described v...
The Friedel-Crafts acylation of anisole with acetic anhydride could be efficiently catalyzed by sui...
WOS: 000325204200122Since alkyl Lewis acids are Bronsted bases, they give a non-acidic reaction medi...
Heteroaromatic compounds, such as thiophenes, pyrroles and furans, were acylated using zeolite Beta,...
Friedel–Crafts reaction is one of the oldest carbon–carbon bond forming processes and is still an at...
To date, great efforts have been made by different research groups to achieve the goal of making the...
Synthesis of fine chemicals and intermediates by using Friedel–Crafts acylations is an important pro...
Chlorothiophenes react with active aromatic compounds in the presence of AlCl3 under mild conditions...
A new highly efficient catalytic procedure for the Friedel–Crafts acylation of electron rich aromati...
Traditional Friedel-Crafts acylation reactions of aromatics suffer from low regio-selectivity toward...
Indian Institute of Chemical Biology, 4 RajaS. C. Mullick Road, Jadavpur, Calcutta-700 032, India M...
The double Friedel–Crafts acylation of readily accessible biaryls with oxalyl chloride delivers the ...
Herein, a method for thioacetalation using BF3SMe2 is presented. The method allows for convenient an...
This paper reports different examples of Friedel-Crafts acylation of various substrates with dicarbo...
The reactivity of thiophene in Diels-Alder reactions is investigated with different maleimide deriva...
A simple and single-step synthesis of 2- and 3-acyl substituted benzothiophenes has been described v...
The Friedel-Crafts acylation of anisole with acetic anhydride could be efficiently catalyzed by sui...