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Updated: Feb 7, 2026

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Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
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Organocatalytic Visible-Light-Driven Metallomimetic Charge Transfer Process: Application in C(sp3)-N Bond Formation
Anukriti Singhal1, Partha Pratim Sen1, Sudipta Raha Roy1
1Department of Chemistry, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016, India.
Organic Letters
|February 5, 2026
Summary
This study introduces a novel visible-light strategy for C-H bond amination in ethers using an organocatalyst. This method achieves sustainable C-N bond formation, expanding photoinduced organic transformations.
Area of Science:
- Organic Chemistry
- Photocatalysis
- Sustainable Chemistry
Background:
- Functionalization of inert C(sp³)-H bonds in ethers remains challenging.
- Traditional methods often require harsh conditions or expensive transition metal catalysts.
- Visible-light photocatalysis offers a sustainable alternative for organic transformations.
Purpose of the Study:
- To develop a visible-light-mediated strategy for the amination of ether C(sp³)-H bonds.
- To utilize an organocatalyst that mimics transition-metal charge transfer.
- To achieve C-H functionalization under mild and sustainable conditions.
Main Methods:
- Employed a polyaromatic odd alternant hydrocarbon-based photocatalyst with Lewis acidic properties.
- Utilized visible light to mediate a charge transfer process.
- Demonstrated the amination of inert C(sp³)-H bonds in ethers.
Main Results:
- Successfully achieved amination of inert C(sp³)-H bonds in ethers via a metallomimetic charge transfer strategy.
- The organocatalytic approach enabled C-H functionalization under mild and sustainable conditions.
- Established a mechanistically distinct platform for light-driven C-N bond formation.
Conclusions:
- A novel visible-light-mediated organocatalytic strategy for ether C-H amination has been demonstrated.
- The metallomimetic charge transfer approach provides a sustainable alternative to traditional methods.
- This work expands the scope of photoinduced organic transformations, particularly in C-N bond formation.
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