Csp <sup>3</sup> –H Bond Carbynoid Functionalization by Photoredox Catalysis

-H carbynoid functionalization of 1,3-dicarbonyl compounds with α-iodionium diazo compounds has been developed to rapidly assemble α,β-diacyl-α,β-unsaturated ketones. This protocol offers a straightforward approach to access β-deuterated-α,β-unsaturated carbonyl molecules via a 1,2-H shift process.

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Publication Details

Journal
Organic Letters
Published
2026-05-18
DOI
https://doi.org/10.1021/acs.orglett.6c01646
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Csp 3 –H Bond Carbynoid Functionalization by Photoredox Catalysis

Wei Zeng, S S Chen, J D Li, Ying Xie et al.
Organic Letters
Cyclopropane Reaction Mechanisms
article

Csp 3 –H Bond Carbynoid Functionalization by Photoredox Catalysis

Wei Zeng, S S Chen, J D Li, Ying Xie, Lixing Shen, J S Peng, Huanfeng Jiang
article en

Abstract

-H carbynoid functionalization of 1,3-dicarbonyl compounds with α-iodionium diazo compounds has been developed to rapidly assemble α,β-diacyl-α,β-unsaturated ketones. This protocol offers a straightforward approach to access β-deuterated-α,β-unsaturated carbonyl molecules via a 1,2-H shift process.

Organic Letters
Key Laboratory of Guangdong Province (CN), Green Chemistry (PL), Sichuan University of Science and Engineering (CN), South China University of Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 10%
Cyclopropane Reaction Mechanisms
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