A new and controllable method for the preparation of unsymmetrical and symmetrical fluorinated benzothiadiazole (FBT)–arene structures that can be applied in organic optoelectronic materials has been developed. The reaction proceeds under mild reaction conditions with high efficiency and shows excellent functional group compatibility, even toward bromide. Fluorinated benzotriazoles also take part in the reaction
An efficient palladium-catalyzed route for the synthesis of benzimidazole-fused phenanthridines from...
A facile synthesis of 1-alkyl benzotriazoles is achieved through fluoride triggered azide-benzyne cy...
Substituted 2,1,3-benzothiadiazole (BTD) is a widely used electron acceptor unit for functional orga...
Arylation in the 4- and 7-positions of 2,1,3-benzothiadiazole (BT) and its monofluoro- (MFBT) and di...
The benzothiadiazole moiety has been extensively exploited as a building block in the syntheses of e...
The Suzuki–Miyaura cross-coupling reaction of 4,7-dibromo-5,6-difluoro-2,1,3-benzothiadiazole with d...
Direct iodination of benzothiazoles under strong oxidative/acidic conditions leads to a mixture of i...
2,1,3-Benzothiadiazole is widely used as a privileged scaffold in pharmaceuticals and organic functi...
An efficient protocol for the palladium-catalyzed direct arene C–H acyloxylation of benzothiadiazole...
<div><p></p><p>A simple, convenient, and efficient new method for synthesis of 2-aryl benzothiazoles...
Palladium nanoparticles, generated in situ efficiently catalyzes direct 2-C-H arylation of benzothia...
Palladium-catalyzed direct arylation of 4-(2-bromophenyl)-2-methylthiazole proceeds with high effici...
The synthetic utility of NaN3 as the azide component in the 3 + 2] annulation with arynes generated ...
An organocatalytic protocol for the syntheses of 2-substituted benzoxazoles and benzothiazoles is de...
Pd-catalyzed direct arylation (DA) reaction conditions have been established for unsubstituted furan...
An efficient palladium-catalyzed route for the synthesis of benzimidazole-fused phenanthridines from...
A facile synthesis of 1-alkyl benzotriazoles is achieved through fluoride triggered azide-benzyne cy...
Substituted 2,1,3-benzothiadiazole (BTD) is a widely used electron acceptor unit for functional orga...
Arylation in the 4- and 7-positions of 2,1,3-benzothiadiazole (BT) and its monofluoro- (MFBT) and di...
The benzothiadiazole moiety has been extensively exploited as a building block in the syntheses of e...
The Suzuki–Miyaura cross-coupling reaction of 4,7-dibromo-5,6-difluoro-2,1,3-benzothiadiazole with d...
Direct iodination of benzothiazoles under strong oxidative/acidic conditions leads to a mixture of i...
2,1,3-Benzothiadiazole is widely used as a privileged scaffold in pharmaceuticals and organic functi...
An efficient protocol for the palladium-catalyzed direct arene C–H acyloxylation of benzothiadiazole...
<div><p></p><p>A simple, convenient, and efficient new method for synthesis of 2-aryl benzothiazoles...
Palladium nanoparticles, generated in situ efficiently catalyzes direct 2-C-H arylation of benzothia...
Palladium-catalyzed direct arylation of 4-(2-bromophenyl)-2-methylthiazole proceeds with high effici...
The synthetic utility of NaN3 as the azide component in the 3 + 2] annulation with arynes generated ...
An organocatalytic protocol for the syntheses of 2-substituted benzoxazoles and benzothiazoles is de...
Pd-catalyzed direct arylation (DA) reaction conditions have been established for unsubstituted furan...
An efficient palladium-catalyzed route for the synthesis of benzimidazole-fused phenanthridines from...
A facile synthesis of 1-alkyl benzotriazoles is achieved through fluoride triggered azide-benzyne cy...
Substituted 2,1,3-benzothiadiazole (BTD) is a widely used electron acceptor unit for functional orga...