Abstract

AbstractCarbon‐Carbon bond forming reactions using Suzuki‐Miyaura cross‐coupling (SMC) technology to construct aryl‐aryl, aryl‐heteroaryl or heteroaryl‐heteroaryl linkages continues to play a vital role in pharmaceuticals, agrochemicals, material science and manufacturing fields. The importance of Suzuki‐Miyaura cross‐coupling which is also reflected in their use in industrial applications, warrants the development of highly efficient catalytic systems that allows the cross‐coupling of economically attractive heteroaryl chlorides. Conversely, the low reactivity of heteroaryl chlorides followed by problems associated with multi‐heteroatom systems amplifies the difficulties involved in SMC procedures. This review focuses on the developments made in the palladium mediated SMC of chloro heterocycles using various palladium/Ligand combinations and highlights the significant improvements achieved by the use of Buchwald's palladium precatalysts.

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