Epoxidation of Chalcone Derivatives under Visible-Light Irradiation: An Organophotoredox Catalytic Approach

Abstract Epoxidation of α,β-unsaturated ketones under visible-light irradiation constitutes a significant chemical transformation with potential applications in the synthesis of epoxypropane derivatives. An organophotoredox catalytic system is herein reported to facilitate efficient aerobic epoxidation. This protocol enables the conversion of α,β-unsaturated ketones into their corresponding epoxy products with moderate to high yields under benign reaction conditions. The methodology demonstrates broad functional-group compatibility, providing a reliable and direct route to a variety of functionalized epoxypropane compounds. Additionally, the absence of heavy metals in this strategy renders it particularly suitable for the pharmaceutical industry, offering a new avenue for the synthesis of epichlorohydrin drugs.

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Journal
Synlett
Published
2024-10-07
DOI
https://doi.org/10.1055/a-2435-6142
Citations
1
Primary Topic
Organic Chemistry Cycloaddition Reactions
Type
article
Field-Weighted Citation Impact
0.25

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article

Epoxidation of Chalcone Derivatives under Visible-Light Irradiation: An Organophotoredox Catalytic Approach

Feifei Wen, Pan Xie, Mengmeng Liu, Wanying Zhang et al.
1 citations
Synlett
Organic Chemistry Cycloaddition Reactions
0.25
article

Epoxidation of Chalcone Derivatives under Visible-Light Irradiation: An Organophotoredox Catalytic Approach

Feifei Wen, Pan Xie, Mengmeng Liu, Wanying Zhang, Xuyang Zhao
article en
1 citations

Abstract

Abstract Epoxidation of α,β-unsaturated ketones under visible-light irradiation constitutes a significant chemical transformation with potential applications in the synthesis of epoxypropane derivatives. An organophotoredox catalytic system is herein reported to facilitate efficient aerobic epoxidation. This protocol enables the conversion of α,β-unsaturated ketones into their corresponding epoxy products with moderate to high yields under benign reaction conditions. The methodology demonstrates broad functional-group compatibility, providing a reliable and direct route to a variety of functionalized epoxypropane compounds. Additionally, the absence of heavy metals in this strategy renders it particularly suitable for the pharmaceutical industry, offering a new avenue for the synthesis of epichlorohydrin drugs.

SynlettVol. 36(07)
Shaanxi University of Science and Technology (CN)
Shaanxi University of Science and Technology
Industry, innovation and infrastructure
Openalex Percentile: Top 48%
Organic Chemistry Cycloaddition Reactions
0.25
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