Conditions for the Suzuki–Miyaura coupling of lithium triisopropyl borates are reported, as well as a procedure for a one-pot lithiation, borylation, and subsequent Suzuki–Miyaura coupling of various heterocycles with aryl halides. These borate species are much more stable toward protodeboronation than the corresponding boronic acids and can conveniently be stored on benchtop at room temperature
The Suzuki–Miyaura cross-coupling reaction is one of the most efficient methods to form new carbon-c...
This thesis describes the steps taken towards the development of a methodology for the synthesis and...
The Suzuki–Miyaura cross-coupling reaction is one of the most efficient methods to form new carbon-c...
A method for the synthesis of biaryls and heterobiaryls from arenes and haloarenes without the inter...
A simple new protocol for the high yielding Suzuki-Miyaura cross-couplings of aryl chlorides with ar...
A simple and mild protocol for the palladium-catalyzed Suzuki reaction of aryl bromides and arylboro...
The first method for achieving alkyl–alkyl Suzuki reactions of unactivated secondary alkyl chlorides...
The use of bis-boronic acid for the direct synthesis of boronic acids has greatly facilitated the tw...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
Chapter 1. Highly active and efficient catalyst systems derived from palladium precatalysts and mono...
A general procedure for the fast Suzuki coupling of major families of heteroaryl bromides was realiz...
Abstract A facile and efficient palladium-catalyzed borylation of aryl (pseudo)halides at room tempe...
Palladium-catalyzed Suzuki–Miyaura cross-coupling reactions of tetrabutylammonium 2-pyridyltriolbora...
The Suzuki–Miyaura cross-coupling reaction is one of the most efficient methods to form new carbon-c...
Palladium-catalyzed Suzuki–Miyaura cross-coupling reactions were studied with potassium Boc-protecte...
The Suzuki–Miyaura cross-coupling reaction is one of the most efficient methods to form new carbon-c...
This thesis describes the steps taken towards the development of a methodology for the synthesis and...
The Suzuki–Miyaura cross-coupling reaction is one of the most efficient methods to form new carbon-c...
A method for the synthesis of biaryls and heterobiaryls from arenes and haloarenes without the inter...
A simple new protocol for the high yielding Suzuki-Miyaura cross-couplings of aryl chlorides with ar...
A simple and mild protocol for the palladium-catalyzed Suzuki reaction of aryl bromides and arylboro...
The first method for achieving alkyl–alkyl Suzuki reactions of unactivated secondary alkyl chlorides...
The use of bis-boronic acid for the direct synthesis of boronic acids has greatly facilitated the tw...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
Chapter 1. Highly active and efficient catalyst systems derived from palladium precatalysts and mono...
A general procedure for the fast Suzuki coupling of major families of heteroaryl bromides was realiz...
Abstract A facile and efficient palladium-catalyzed borylation of aryl (pseudo)halides at room tempe...
Palladium-catalyzed Suzuki–Miyaura cross-coupling reactions of tetrabutylammonium 2-pyridyltriolbora...
The Suzuki–Miyaura cross-coupling reaction is one of the most efficient methods to form new carbon-c...
Palladium-catalyzed Suzuki–Miyaura cross-coupling reactions were studied with potassium Boc-protecte...
The Suzuki–Miyaura cross-coupling reaction is one of the most efficient methods to form new carbon-c...
This thesis describes the steps taken towards the development of a methodology for the synthesis and...
The Suzuki–Miyaura cross-coupling reaction is one of the most efficient methods to form new carbon-c...