Recent Advances in the Photochemical Synthesis of Esters

Abstract Photocatalysis has recently emerged as a powerful synthetic tool for making a variety of carbon‐carbon and carbon‐heteroatom bonds. The development of esterification reactions induced by light is an atom economical and energy efficient alternative to traditional methods for the synthesis of esters, with benefits including mild reaction conditions, high chemical yields, and wide functional group tolerance. This review summarizes recent progress made in this green methodology, including mechanisms of action, substrate scope, limitations and future prospects.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-02-06
DOI
https://doi.org/10.1002/ejoc.202401398
Citations
5
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
4.68
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article

Recent Advances in the Photochemical Synthesis of Esters

Hong‐Xi Li, David James Young, Da‐Liang Zhu, Yanqing Wang et al.
5 citations
European Journal of Organic Chemistry
Chemical Synthesis and Reactions
4.68
article

Recent Advances in the Photochemical Synthesis of Esters

Hong‐Xi Li, David James Young, Da‐Liang Zhu, Yanqing Wang, Jie Li
article en
5 citations

Abstract

Abstract Photocatalysis has recently emerged as a powerful synthetic tool for making a variety of carbon‐carbon and carbon‐heteroatom bonds. The development of esterification reactions induced by light is an atom economical and energy efficient alternative to traditional methods for the synthesis of esters, with benefits including mild reaction conditions, high chemical yields, and wide functional group tolerance. This review summarizes recent progress made in this green methodology, including mechanisms of action, substrate scope, limitations and future prospects.

European Journal of Organic ChemistryVol. 28(12)
Soochow University (CN), Analysis and Testing Centre (CN), Yancheng Teachers University (CN), University of Glasgow (GB)
Openalex Percentile: Top 6%
Chemical Synthesis and Reactions
4.68
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