Using asymmetric catalysis to simultaneously form carbon–carbon bonds and generate single isomer products is strategically important. Suzuki-Miyaura cross-coupling is widely used in the academic and ...

It is defined as the cross-coupling of organoboron compounds with organic halogen containing molecules, catalyzed by palladium. The reaction is important to organic chemistry because it forms ...

The Suzuki-Miyaura cross-coupling is an invaluable C-C bond forming reaction, but it can be limited by the availability, isolation and stability of the boronate starting materials. This has led to the ...

It’s hard to improve on a classic. But Richard Y. Liu was eager to take on that challenge. Cross-coupling reactions, including Suzuki-Miyaura coupling and Buchwald-Hartwig amination, are some of the ...

Most of today's use of transition metal–catalyzed cross-coupling chemistry relies on expensive quantities of palladium (Pd). Here we report that nanoparticles formed from inexpensive FeCl3 that ...

The Suzuki-Miyaura transformation is a classic way to form carbon-carbon bonds. In the reaction, a palladium catalyst typically couples two classes of molecules, aryl halides and aryl boronate ...