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.

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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

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article

Asymmetric Synthesis of Tetrahydrofurans with Vicinal Stereocenters by RhII/RuII Relay Catalysis

Fangjie Liu, Baihua Ye, Xuejiao Li
The Journal of Organic Chemistry
Cyclopropane Reaction Mechanisms
article

Asymmetric Synthesis of Tetrahydrofurans with Vicinal Stereocenters by RhII/RuII Relay Catalysis

Fangjie Liu, Baihua Ye, Xuejiao Li
article en

Abstract

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.

The Journal of Organic ChemistryVol. 90(18)
ShanghaiTech University (CN)
ShanghaiTech University
Openalex Percentile: Top 93%
Cyclopropane Reaction Mechanisms
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