The palladium-catalyzed reaction of aryl halide and boronic acid for the formation of C–C bonds so-called Suzuki–Miyaura cross-coupling reaction has many applications in Modern Synthetic Organic Chemistry. In 2013, we emphasized the applications of the intramolecular Suzuki cross-coupling reaction in cyclization and heterocyclization. Due to a plethora relevant papers appeared in the chemical literature, herein, we wish to cover by updating our previous review, the applications of the intramolecular Suzuki cross-coupling reaction in cyclization and heterocyclization leading to various homocyclic and heterocyclic compounds reported during a period of 2013 to 2018
The Suzuki-Miyaura reaction (SMR), involving the coupling of an organoboron reagent and an organic h...
[[abstract]]In this mini-review, we present a summary of our recent work in the field of palladium-c...
The past decades in organic chemistry have witnessed significant improvements in synthetic efficienc...
Palladium-catalyzed cross-coupling reactions are nowadays essential in organic synthesis for the con...
In this review, the various groups have reported significant contributions in Suzuki–Miyaura (SM) co...
The Suzuki-Miyaura reaction (SMR), involving the coupling of an organoboron reagent and an organic h...
While the Suzuki coupling has gained paramount importance, the basic set-up of the reaction has rema...
Our group has developed a strategy for the synthesis of benzofused carbocycles and heterocycles thro...
Since the original reports of Suzuki-Miyaura on the coupling of vinyl or aryl boronic acids with vin...
Our group has developed a strategy for the synthesis of benzofused carbocycles and heterocycles thro...
The paper describes the Suzuki cross-coupling of a variety of N and C-3 substituted 5-bromoindazoles...
The paper describes the Suzuki cross-coupling of a variety of N and C-3 substituted 5-bromoindazoles...
The Suzuki-Miyaura reaction (SMR), involving the coupling of an organoboron reagent and an organic h...
The importance of palladium-catalyzed cross coupling reactions in contemporary organic synthesis is ...
Transition metal-catalyzed cross-coupling reaction has become a useful methodology for the formation...
The Suzuki-Miyaura reaction (SMR), involving the coupling of an organoboron reagent and an organic h...
[[abstract]]In this mini-review, we present a summary of our recent work in the field of palladium-c...
The past decades in organic chemistry have witnessed significant improvements in synthetic efficienc...
Palladium-catalyzed cross-coupling reactions are nowadays essential in organic synthesis for the con...
In this review, the various groups have reported significant contributions in Suzuki–Miyaura (SM) co...
The Suzuki-Miyaura reaction (SMR), involving the coupling of an organoboron reagent and an organic h...
While the Suzuki coupling has gained paramount importance, the basic set-up of the reaction has rema...
Our group has developed a strategy for the synthesis of benzofused carbocycles and heterocycles thro...
Since the original reports of Suzuki-Miyaura on the coupling of vinyl or aryl boronic acids with vin...
Our group has developed a strategy for the synthesis of benzofused carbocycles and heterocycles thro...
The paper describes the Suzuki cross-coupling of a variety of N and C-3 substituted 5-bromoindazoles...
The paper describes the Suzuki cross-coupling of a variety of N and C-3 substituted 5-bromoindazoles...
The Suzuki-Miyaura reaction (SMR), involving the coupling of an organoboron reagent and an organic h...
The importance of palladium-catalyzed cross coupling reactions in contemporary organic synthesis is ...
Transition metal-catalyzed cross-coupling reaction has become a useful methodology for the formation...
The Suzuki-Miyaura reaction (SMR), involving the coupling of an organoboron reagent and an organic h...
[[abstract]]In this mini-review, we present a summary of our recent work in the field of palladium-c...
The past decades in organic chemistry have witnessed significant improvements in synthetic efficienc...