Pyridine is a ubiquitous building block for the design
of very
diverse ligand platforms, many of which have become indispensable
for catalytic transformations. Nevertheless, the isosteric pyrazine,
pyrimidine, and triazine congeners have enjoyed thus far a less privileged
role in ligand design. In this review, several applications of such
fragments in the design of new catalysts are presented. In a significant
number of cases described, diazine- and triazine-based ligands either
outperform their pyridine congeners or offer alternative catalytic
pathways which enable new reactivities. The potential opportunities
unlocked by using these building blocks in ligand design are discussed,
and the origin of the enhanced catalytic activity is highlighted where
mechanistic studies are available.