Lecture
This lecture covers various asymmetric reactions in organic chemistry, including hydrogenation, allylation, conjugate reduction, and epoxide opening. It explores key concepts such as dual activation, stereodivergence, and kinetic resolution. The instructor discusses the mechanisms, catalysts, and selectivity involved in these reactions, showcasing the importance of ligand design and metal coordination. Examples from literature, such as the Sharpless Epoxidation and the Noyori Hydrogenation, are used to illustrate the principles behind these reactions.