Related Experiment Video
Updated: Jan 6, 2026

Sequence-specific Labeling of Nucleic Acids and Proteins with Methyltransferases and Cofactor Analogues
Published on: November 22, 2014
Recent Advances in Single-Electron-Transfer-Mediated Carbonylation.
Le-Cheng Wang1,2, Hefei Yang1,2, Zhen-Wei Liu1,2
1Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Single-electron transfer (SET) carbonylation offers an alternative to traditional two-electron transfer (TET) methods. SET provides milder conditions, enhanced selectivity, and broader substrate compatibility for synthesizing carbonyl compounds.
Area of Science:
- Organic Chemistry
- Catalysis
- Synthetic Chemistry
Background:
- Carbonylation reactions are vital for synthesizing carbonyl compounds.
- Two-electron transfer (TET) processes are widely used but have limitations.
- Single-electron transfer (SET) offers an alternative with advantages over TET.
Purpose of the Study:
- To provide a comprehensive review of SET-mediated carbonylation chemistry.
- To highlight mechanistic insights, catalytic systems, and synthetic applications.
- To establish a foundation for future research in SET carbonylation.
Main Methods:
- Review of scientific literature from 2000 to July 2025.
- Analysis of mechanistic pathways in SET carbonylation.
- Categorization of catalytic systems and synthetic applications.
Main Results:
- SET carbonylation bypasses traditional oxidative addition.
- Highly reactive radical intermediates are generated under milder conditions.
- SET offers enhanced selectivity and broader substrate compatibility compared to TET.
Conclusions:
- SET-mediated carbonylation presents a powerful alternative to TET methods.
- This approach enables more versatile and efficient synthesis of carbonyl compounds.
- Further exploration of SET strategies is encouraged for novel reactivity.
Related Concept Videos
Carbocations
Nucleophilic Addition to the Carbonyl Group: General Mechanism
A stronger nucleophile can directly attack the electrophilic center, the carbonyl carbon. The HOMO orbital of the nucleophile interacts with the LUMO (π* antibonding) orbital present on the carbonyl carbon. This interaction breaks the π bond and shifts the π...
Preparation of Carboxylic Acids: Carboxylation of Grignard Reagents
Nucleophilic Acyl Substitution of Carboxylic Acid Derivatives
Electrophilic Aromatic Substitution: Friedel–Crafts Acylation of Benzene
Conjugate Addition to α,β-Unsaturated Carbonyl Compounds

