metaselective

Metaselective describes a property of a chemical reaction, catalyst, or condition that preferentially yields meta-substituted products, especially in aromatic systems. It denotes meta-regioselectivity, distinguishing it from ortho- or para-substitution outcomes. The term appears in discussions of organic synthesis where standard directing effects favor other positions, and researchers seek to access meta-substituted arenes through specialized strategies.

Achieving metaselectivity often requires design elements that override conventional directing effects. Common approaches include transient or removable directing groups or templates that orient a metal catalyst to the meta position, as well as ligand-controlled or metal-ligand cooperative catalysis. In some cases, multi-component catalytic cycles enable remote or distal functionalization, producing meta-functionalized arenes without a permanently installed directing group. Non-directed methods and relay or sequence-based strategies also contribute to meta-selectivity in suitable substrates.

Applications of metaselective methods span pharmaceutical, agrochemical, and materials science contexts, where meta-substituted arenes are desired but difficult to access with traditional directivity. The ability to install substituents at the meta position expands synthetic routes and can streamline the construction of complex molecules.

In the literature, metaselective is sometimes used interchangeably with meta-selective, although the latter term is more common in contemporary writing. Ongoing research aims to broaden substrate scope, improve efficiency and enantioselectivity, and simplify the use and removal of directing templates to make metaselective strategies more widely practical.