Gold(I)-Catalyzed 1,6-Enyne Single-Cleavage Rearrangements: The Complete Picture
Eduardo García‐Padilla, Feliu Maseras, Antonio M. Echavarren
Abstract
High Resolution Image Download MS PowerPoint Slide We identify the factors that rule the selectivity in single-cleavage skeletal rearrangements promoted by gold(I) catalysts. We find that stereoconvergence is enabled by a rotational equilibrium when electron-rich substituents are used. The anomalous Z- selective skeletal rearrangement is found to be due to electronic factors, whereas endo -selectivity depends on both steric and electronic factors.
Topics & Concepts
Steric effectsCleavage (geology)SelectivityCatalysisChemistryEnyneStereochemistryElectronic effectPhotochemistryOrganic chemistryMaterials scienceComposite materialFracture (geology)Catalytic Alkyne ReactionsCatalysis for Biomass ConversionCyclopropane Reaction Mechanisms