International audienceWe designed a new, user-friendly oxidative dual heterogeneous catalytic system capable of promoting polysubstituted pyridines as unique products from simple activated Michael acceptors, 1,3-dicarbonyls and ammonium acetate. This metal-free environmentally-respectful and totally regioselective domino reaction proved to be a great strategy to access bi- and tri-aryl type pyridines as well as challenging bi- and tri-heteroaryl type pyridines in a single operation
The catalytic reactions of acetylene and dimethyl ketone with ammonia for the synthesis of pyridine ...
A low loading of a quinine-derived squaramide efficiently catalyzes the triple-domino Michael/aza-He...
A highly regioselective acid-catalyzed three-component reaction of 2-aminopyridine and 3-phenylpropi...
International audienceWe designed a new, user-friendly oxidative dual heterogeneous catalytic system...
International audienceA metal-free and completely regioselective three-component synthesis of highly...
International audienceA simple metal-free, step-economic and selective access to pyr- idines from re...
International audienceα-Ketocarbonyls have been shown for the first time to be versatile partners in...
The pyridine heterocycle continues to play a vital role in the development of human medicines. More ...
A base-mediated three-component tandem reaction for the synthesis of multisubstituted pyrimidines fr...
The pyridine heterocycle continues to play a vital role in the development of human medicines. More ...
An efficient heterogeneous copper(I)-catalyzed three-component tandem cyclization of ketoxime acetat...
The interplay and synergistic cooperation between homogeneous and heterogeneous catalyst systems is ...
The olefin cross-metathesis reaction provides a rapid and efficient method for the synthesis of α,β-...
A variety of tri- and tetrasubstituted pyridines are prepared by new one-pot processes, developed by...
The catalytic reactions of acetylene and dimethyl ketone with ammonia for the synthesis of pyridine ...
A low loading of a quinine-derived squaramide efficiently catalyzes the triple-domino Michael/aza-He...
A highly regioselective acid-catalyzed three-component reaction of 2-aminopyridine and 3-phenylpropi...
International audienceWe designed a new, user-friendly oxidative dual heterogeneous catalytic system...
International audienceA metal-free and completely regioselective three-component synthesis of highly...
International audienceA simple metal-free, step-economic and selective access to pyr- idines from re...
International audienceα-Ketocarbonyls have been shown for the first time to be versatile partners in...
The pyridine heterocycle continues to play a vital role in the development of human medicines. More ...
A base-mediated three-component tandem reaction for the synthesis of multisubstituted pyrimidines fr...
The pyridine heterocycle continues to play a vital role in the development of human medicines. More ...
An efficient heterogeneous copper(I)-catalyzed three-component tandem cyclization of ketoxime acetat...
The interplay and synergistic cooperation between homogeneous and heterogeneous catalyst systems is ...
The olefin cross-metathesis reaction provides a rapid and efficient method for the synthesis of α,β-...
A variety of tri- and tetrasubstituted pyridines are prepared by new one-pot processes, developed by...
The catalytic reactions of acetylene and dimethyl ketone with ammonia for the synthesis of pyridine ...
A low loading of a quinine-derived squaramide efficiently catalyzes the triple-domino Michael/aza-He...
A highly regioselective acid-catalyzed three-component reaction of 2-aminopyridine and 3-phenylpropi...