| Literature DB >> 23525350 |
Nathan C Thacker1, Shin A Moteki, James M Takacs.
Abstract
Results are reported for the catalytic asymmetric hydrogenation of two prototypical substrates with a series of more than 150 closely related supramolecular catalysts differing in only their ligand/catalyst scaffold. These modular catalysts are constructed from four subunits and vary widely in their reactivity (no reaction to quantitative yield) and enantioselectivity (racemic to 96% ee). Analysis of the ligand/catalyst scaffold optimization data reveals how each subunit contributes to the effectiveness of the modular supramolecular catalyst. The results suggest that a balance between key elements of rigidity and flexibility is required for the successful catalysts and, moreover, that this balance is required to enable effective fine-tuning via catalyst scaffold optimization.Entities:
Keywords: asymmetric catalysis; asymmetric hydrogenation; rhodium-catalyzed; self-assembled ligands; self-assembly; supramolecular catalysis
Year: 2012 PMID: 23525350 PMCID: PMC3601680 DOI: 10.1021/cs300465u
Source DB: PubMed Journal: ACS Catal Impact factor: 13.084