Deciphering the Keys for High Enantioselectivity in Hypervalent Iodine-Catalyzed 1,2-Difunctionalization: Improved Synthesis of Ishihara–Muñiz Precatalysts
Eric Cots, Jeroen Rintjema, Fernando Bravo, Kilian Muñiz
Abstract
In the course of upscaling the synthesis of enantiopure aryliodine precatalysts, we detected an unreported meso form of the catalysts for the first time. A new scalable route was developed to avoid epimerization of the lactamide arms, providing syntheses of the precatalysts that are both more effective and much less time-consuming. The catalysts obtained with these synthetic procedures have been employed in some published reactions, reaching the maximum ee ever reported.
Topics & Concepts
Enantiopure drugHypervalent moleculeChemistryCatalysisIodineEpimerCombinatorial chemistryOrganic chemistryEnantioselective synthesisOxidative Organic Chemistry ReactionsAsymmetric Synthesis and CatalysisCatalytic C–H Functionalization Methods