A new approach for electrooxidative coupling of aromatic compounds and primary alkylamines bearing a functional group such as a hydroxyl group and an amino group was developed. The key to the success of the transformation is heterocyclization of functional primary alkylamines. Treatment of primary alkylamines bearing a functional group with nitriles or their equivalents gives the corresponding heterocycles. The electrochemical oxidation of aromatic substrates in the presence of the heterocycles followed by chemical reaction under nonoxidative conditions gave the desired coupling products
An effective Friedel–Crafts alkylation reaction of electron-rich aromatics with <i>N</i>-vinylamides...
Abstract Direct functionalization of C(sp3)–H bonds allows rapid access to valuable products, starti...
The functionalization of aminoheterocycles via a pyrylium tetrafluoroborate reagent (Pyry‐BF<sub>4</...
Electrochemical radical cascade cyclization has been recognized as a powerful, straightforward, and ...
Methods and techniques that can be used to perform various chemical transformations in an environmen...
We have developed a new method for C–H amination of aromatic compounds based on electrochemical oxid...
The use of electrochemistry in synthesis is a relatively unexplored area of organic chemistry that i...
Radical cyclisation is rapidly becoming an important method for the formation of cyclic systems. Hen...
Synthesis of heterocycles from 1,2-diarylalkene derivatives through electrosynthesis under metal- an...
The review summarizes for the first time the poorly studied electrooxidative functionalization of py...
Radical cyclization continues to be a central methodology for the preparation of natural products co...
A new sequential three-component heterocyclization was developed by reacting aromatic and heterocycl...
Diaryl alcohol moieties are widespread in pharmaceuticals. Existing methods for the synthesis of dia...
We investigated the reductive intramolecular cyclization of bromopropargyl ethers derivatives, cata...
0022-3263International audienceA general efficient electrochemical method for the preparation of ary...
An effective Friedel–Crafts alkylation reaction of electron-rich aromatics with <i>N</i>-vinylamides...
Abstract Direct functionalization of C(sp3)–H bonds allows rapid access to valuable products, starti...
The functionalization of aminoheterocycles via a pyrylium tetrafluoroborate reagent (Pyry‐BF<sub>4</...
Electrochemical radical cascade cyclization has been recognized as a powerful, straightforward, and ...
Methods and techniques that can be used to perform various chemical transformations in an environmen...
We have developed a new method for C–H amination of aromatic compounds based on electrochemical oxid...
The use of electrochemistry in synthesis is a relatively unexplored area of organic chemistry that i...
Radical cyclisation is rapidly becoming an important method for the formation of cyclic systems. Hen...
Synthesis of heterocycles from 1,2-diarylalkene derivatives through electrosynthesis under metal- an...
The review summarizes for the first time the poorly studied electrooxidative functionalization of py...
Radical cyclization continues to be a central methodology for the preparation of natural products co...
A new sequential three-component heterocyclization was developed by reacting aromatic and heterocycl...
Diaryl alcohol moieties are widespread in pharmaceuticals. Existing methods for the synthesis of dia...
We investigated the reductive intramolecular cyclization of bromopropargyl ethers derivatives, cata...
0022-3263International audienceA general efficient electrochemical method for the preparation of ary...
An effective Friedel–Crafts alkylation reaction of electron-rich aromatics with <i>N</i>-vinylamides...
Abstract Direct functionalization of C(sp3)–H bonds allows rapid access to valuable products, starti...
The functionalization of aminoheterocycles via a pyrylium tetrafluoroborate reagent (Pyry‐BF<sub>4</...