Abstract
AbstractStereodivergent catalysis has emerged as a compelling strategy for achieving stereochemical diversity in small-molecule library design and natural product synthesis. In this short review, key examples of pioneering catalytic carbon–carbon bond-forming transformations that provide access to all stereoisomers of a given product are presented. Current trends and future directions in the field are discussed, highlighting ongoing initiatives to enhance the efficiency and broaden the scope of stereodivergent methodologies.1 Introduction2 Mono-catalysis2.1 Change of Reaction Conditions2.2 Change of Catalyst3 Multi-catalysis3.1 Bifunctional Catalysis3.2 Sequential/Cascade Catalysis3.3 Synergistic/Cooperative Catalysis4 Conclusions and Outlook
Funder
New York University Abu Dhabi