Asymmetric & Chiral Synthesis
Asymmetric and chiral synthesis form the foundation of modern molecular design, ensuring precise control over stereochemistry in biologically active compounds. Advances in enantioselective catalysis, chiral auxiliaries, stereodivergent strategies, and biocatalytic methods have transformed the ability to access single-enantiomer molecules essential for drug development and fine chemicals. Innovations in chiral ligand architecture, asymmetric hydrogenation, organocatalytic cascade reactions, and atroposelective transformations enhance both efficiency and selectivity. Mechanistic understanding of chiral induction and transition-state stabilization supports the development of broader substrate scopes and greener methodologies. Emerging photochemical and electrochemical chiral catalysts introduce new activation modes that enable transformations under milder conditions. These developments collectively elevate the precision and sustainability of stereoselective synthesis.
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