Enantioselective Contrathermodynamic Olefin Isomerization
A light-driven method for the enantioselective contrathermodynamic positional isomerization of olefins based on excited-state electron transfer is reported. Sequential oxidation and deprotonation of a tetrasubstituted enol ether generates an allylic radical which is captured by a Cr(II) cocatalyst bearing a chiral bioxazoline (BiOX) ligand. Regio- and enantioselective protodemetalation of the nascent Cr(III) allyl complex by methanol yields the terminal olefin product with enantioselectivities of up to 95:5 er. Kinetic and isotopic labeling studies support an enantiodetermining protodemetalation and reveal the presence of two primary KIEs within the same catalytic manifold.
Authors
- Kuo Zhao (ORCID: https://orcid.org/0000-0002-1451-7313)
- Robert R. Knowles (ORCID: https://orcid.org/0000-0003-1044-4900)
- Eve Yuanwei Xu (ORCID: https://orcid.org/0000-0002-7212-3363)
- Sumin Lee (ORCID: https://orcid.org/0000-0002-6068-3929)
- Bianca L Imbriaco
Institutions
- Princeton University (US)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-05-01
- DOI
- https://doi.org/10.1021/jacs.6c04825
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Institute of General Medical Sciences
- National Science Foundation Graduate Research Fellowship Program