Inefficient multi-step synthesis of substituted heterocycles increases manufacturing costs and reduces purity. These processes utilize specific regioselective substitution patterns to streamline the production of complex pharmaceutical intermediates.
Uncontrolled substitution patterns during the synthesis of complex cyanocyclopropyl and oxazolidinone derivatives lead to poor isomeric purity. Achieving precise site-specific modification prevents yield loss and costly separation of structural isomers.