The stereochemical course of the Pd–catalyzed Suzuki-Miyaura cross-coupling of α-substituted, enantioenriched allylic boronic esters with phenyl iodide has been examined. The secondary boronic esters were prepared in both ...

The advent of the Suzuki–Miyaura cross–coupling reaction and its significance to the synthesis of new carbon–carbon bonds has increased the demand for efficient routes to organoboron starting materials. C–H borylation ...

Herein I describe a model study to determine the feasibility of organic hydride donors as a source of hydride in the regeneration of ammonia borane. Hydride transfer was observed in the model system comprised of Hantzsch ...

The palladium-catalyzed Suzuki-Miyaura cross-coupling, in which a carbon-carbon bond is formed between an organohalide or pseudo-halide electrophile and an organoboron nucleophile, has developed into one of the most widely ...

Little attention has been given to the formation of the putative PdL2 species required for Pd-catalyzed cross-coupling reactions. Active species are generally difficult to store due to air-sensitivity and are therefore ...

The Suzuki-Miyaura Cross-Coupling of aryl halides and aryl boronic esters has become one of the most important and oft used C-C bond forming reactions in industry and academia alike. Recently, substantial effort has been ...

Until recently, secondary organoboronic esters were not viable substrates in the Suzuki-Miyaura cross-coupling reaction; however under recently reported conditions from the Crudden group1, which includes the addition of ...