A novel rearrangement process involving the migration of trimethylstannanyl or trimethylsilanyl groups around the thiazole ring provides access to either 2- or 5-metallated thiazoles by tuning the reaction conditions. The proposed mechanism, based on experimental evidence, is characterized by the catalytic role of thiazole bisadducts as metal-transfer agents. \ua9 2007 Elsevier Ltd. All rights reserved
The reaction between 3-amino-3-(dialkylamino)propenenitriles 1 and sodium thiocyanate in presence of...
International audience2-Thiazolines are important building blocks in organic synthesis and are of gr...
3-Pyridyl-4-alkyl (or aryl)-1,2,4-oxadiazole-5(4H)-thiones are prepared by the reaction of N-alkyl (...
A novel rearrangement process involving the migration of trimethylstannanyl or trimethylsilanyl grou...
The equilibrium in the reversible rearrangement of 5-methyl-1,2,3- thiadiazole-4-carbothioamides int...
Thiazoles are ubiquitous heterocycles that occupy an important place in medicinal chemistry, servin...
The azido transfer procedure of heteroaryllithium and tosyl azide was used to synthesize selected 2-...
An efficient regioselective arylation of thiazole derivatives via Pd-catalyzed C-H activation is rep...
A new strategy for thiazoles via copper-catalyzed [3+1+1]-type condensation reaction from oximes, an...
International audiencePd-catalyzed direct arylation of 2-alkylthiazoles is a well-known reaction aff...
Department of Chemistry, University of Calcutta, University College of Science, Kolkata-700 009, Ind...
International audienceThe versatile functionalization of thiazoles and benzothiazoles at different l...
Regioselective a-bromination of (Z)-5-substituted-2-alkylidene-4-oxothiazolidine derivatives affords...
For many decades, the thiazole moiety has been an important heterocycle in the world of chemistry. T...
Bi- and terthiazolyl have been prepared in high yields by cross-coupling of trimethylstannylthiazole...
The reaction between 3-amino-3-(dialkylamino)propenenitriles 1 and sodium thiocyanate in presence of...
International audience2-Thiazolines are important building blocks in organic synthesis and are of gr...
3-Pyridyl-4-alkyl (or aryl)-1,2,4-oxadiazole-5(4H)-thiones are prepared by the reaction of N-alkyl (...
A novel rearrangement process involving the migration of trimethylstannanyl or trimethylsilanyl grou...
The equilibrium in the reversible rearrangement of 5-methyl-1,2,3- thiadiazole-4-carbothioamides int...
Thiazoles are ubiquitous heterocycles that occupy an important place in medicinal chemistry, servin...
The azido transfer procedure of heteroaryllithium and tosyl azide was used to synthesize selected 2-...
An efficient regioselective arylation of thiazole derivatives via Pd-catalyzed C-H activation is rep...
A new strategy for thiazoles via copper-catalyzed [3+1+1]-type condensation reaction from oximes, an...
International audiencePd-catalyzed direct arylation of 2-alkylthiazoles is a well-known reaction aff...
Department of Chemistry, University of Calcutta, University College of Science, Kolkata-700 009, Ind...
International audienceThe versatile functionalization of thiazoles and benzothiazoles at different l...
Regioselective a-bromination of (Z)-5-substituted-2-alkylidene-4-oxothiazolidine derivatives affords...
For many decades, the thiazole moiety has been an important heterocycle in the world of chemistry. T...
Bi- and terthiazolyl have been prepared in high yields by cross-coupling of trimethylstannylthiazole...
The reaction between 3-amino-3-(dialkylamino)propenenitriles 1 and sodium thiocyanate in presence of...
International audience2-Thiazolines are important building blocks in organic synthesis and are of gr...
3-Pyridyl-4-alkyl (or aryl)-1,2,4-oxadiazole-5(4H)-thiones are prepared by the reaction of N-alkyl (...