Multifunctional chiral silanol ligands for enantioselective catalysis
We report transition metal catalysis using novel chiral metal-chelating ligands featuring a silanol coordinating group and peptide-like aminoamide scaffold. The catalytic properties of the silanol ligand are demonstrated through an enantioselective Cu-catalyzed N-H insertion affording unnatural amino acid derivatives in high selectivity. Our investigations into the silanol coordination mode include DFT calculations, ligand structure investigations, and X-ray structure analyses, which support the formation of an H-bond stabilized silanol-chelating copper carbenoid complex. A π-π stacking interaction revealed by DFT calculations is proposed to enable selectivity for aryl diazoacetate substrates, overcoming some of the traditional limitations of using these substrates.
Authors
- Yun‐Pu Chang (ORCID: https://orcid.org/0000-0003-2866-1735)
- Annaliese K. Franz (ORCID: https://orcid.org/0000-0002-4841-2448)
- Turki M. Alturaifi (ORCID: https://orcid.org/0000-0002-6379-1669)
- Peng Liu (ORCID: https://orcid.org/0000-0002-8188-632X)
- James C. Fettinger (ORCID: https://orcid.org/0000-0002-6428-4909)
- Kevin Blanco-Herrero
Institutions
- University of Pittsburgh (US)
- University of California, Davis (US)
Publication Details
- Journal
- Chemical Science
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5sc02528a
- Citations
- 1
- Primary Topic
- Asymmetric Synthesis and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.94
Funders
- National Science Foundation
- University of Pittsburgh
- National Institutes of Health
- University of California, Davis
- Center for Research Computing, University of Pittsburgh
- Office of Advanced Cyberinfrastructure
- Division of Chemistry