The Suzuki-Miyaura reaction is a well-known chemical process in which a reaction between organic boronic acids and aryl halides leads to the synthesis of "biaryl" compounds, which are important components of various drugs and chemical products. This is also called cross-coupling, as two aryl molecules are combined, or cross-coupled, in this process. Because the organic aromatic molecules—which are formed as a result of this reaction—have various applications, such as in solvents and drugs, finding a way of optimizing the existing cross-coupling reactions is crucial. This is why, in a new study published in ACS Catalysts, a team of scientists from Japan, including Junior Assoc Prof Yuichiro Mutoh and Prof Shinichi Saito of Tokyo University of Science, wanted to check if this reaction can be made more efficient.
