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May 20, 2026Organic Letters0 citations

Construction of β-Heteroarylated Aliphatic Aldehydes via Pd-Catalyzed and Ag-Mediated Redox-Relay Oxidative Heck Reactions

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JLJunxiang Liu苟苟练TSTao Sun

Key Points

  • To develop a method for synthesizing β-heteroarylated aliphatic aldehydes using Pd-catalyzed and Ag-mediated reactions.
  • Utilized Pd-catalyzed and Ag-mediated redox-relay oxidative Heck reactions with furans/thiophenes and cis-alkenols.
  • Conducted parallel kinetic isotope effect experiments to investigate the reaction mechanism.
  • Analyzed fluorescence properties of synthesized materials for use in cellular imaging.
  • Identified the rate-determining step involves C-H bond breaking in the heterocycle.
  • Achieved successful synthesis across a broad substrate scope for various aldehyde derivatives.
  • Demonstrated the potential of novel fluorescent materials in lysosome targeting and two-channel emission-intensity-ratio imaging of HeLa cells.

Abstract

Herein, we report the first example of Pd-catalyzed and Ag-mediated redox-relay oxidative Heck reactions of furans/thiophenes with cis-alkenols to construct β-heteroarylated aliphatic aldehydes. Parallel kinetic isotope effect (KIE) experiments reveal that C-H bond breaking of the heterocycle might be involved in the rate-determining step. This approach features a broad substrate scope while enabling straightforward access to fluoroboron fluorescent and anti-Kasha dual-emission fluorescent materials. The novel fluorescent materials can selectively accumulate in lysosomes. In addition, the nanoparticles of the anti-Kasha dual-emission material can be used for two-channel emission-intensity-ratio imaging of HeLa cells, which favors observing the local cellular information and intercellular structures.

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Cite This Study

Liu et al. (2026) studied this question.

synapsesocial.com/papers/6a0d5064f03e14405aa9c159https://doi.org/10.1021/acs.orglett.6c01412
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