Asymmetric Synthesis of Tetrahydrofurans with Vicinal Stereocenters by Rh<sup>II</sup>/Ru<sup>II</sup> Relay Catalysis
CpRu-catalyzed asymmetric allylic alkylation serves as a versatile synthetic tool but remains underexplored. Herein, we report a relay system combining achiral Rh<sub>2</sub>(OAc)<sub>4</sub> and a chiral pyridine-oxazoline-ligated Cp*Ru catalyst for asymmetric coupling of cinnamyl chlorides with diazo esters, generating silyl enol ethers <i>in situ</i> as key nucleophilic intermediates. This strategy affords chiral tetrahydrofuran derivatives with two vicinal stereocenters. Catalyst compatibility, excellent regioselectivity, and good enantioselectivity highlight its potential. Computational studies reveal the crucial role of Ru-centered chirality in reaction control.
Authors
- Fangjie Liu (ORCID: https://orcid.org/0000-0002-5207-5157)
- Baihua Ye (ORCID: https://orcid.org/0000-0001-9369-2656)
- Xuejiao Li (ORCID: https://orcid.org/0000-0002-2250-0300)
Institutions
- ShanghaiTech University (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2025-04-25
- DOI
- https://doi.org/10.1021/acs.joc.5c00324
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- ShanghaiTech University