UT Dallas researchers developed a new chemical reaction to synthesize enantiomers of mirror molecules, enabling selective production of versions with desired biological effects for potential use in treating cancer, infection, depression, and more. The method, published in 'Science,' involves adding prenyl groups to enones using a new catalyst, allowing for scalable, efficient synthesis of pure enantiomers. This breakthrough could impact drug discovery by facilitating the production of natural product analogs with enhanced potency and selectivity.