Electrochemical Esterification Reaction of Alkyne Aldehyde with Alcohols Mediated by Carbene and Iodine

Abstract A new type of alkyne esterification was developed under electrochemical conditions using alkyne aldehydes and alcohol compounds as starting materials and carbene and iodine as mediators. Through this method, external oxidants and transition metals are excluded and the alkyne bond is fully preserved. This approach is compatible with a wide range of substrates and various functional groups and provides a green and mild new route for directly converting alkyne aldehydes into alkyne esters.

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Publication Details

Journal
ChemCatChem
Published
2024-11-11
DOI
https://doi.org/10.1002/cctc.202401418
Citations
1
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.25

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article

Electrochemical Esterification Reaction of Alkyne Aldehyde with Alcohols Mediated by Carbene and Iodine

Ying‐Ming Pan, Kai‐Wei Chen, Haitao Tang, Fei‐Hu Cui et al.
1 citations
ChemCatChem
Oxidative Organic Chemistry Reactions
0.25
article

Electrochemical Esterification Reaction of Alkyne Aldehyde with Alcohols Mediated by Carbene and Iodine

Ying‐Ming Pan, Kai‐Wei Chen, Haitao Tang, Fei‐Hu Cui, Guo‐Ao Wang, Shu‐Hui Li
article en
1 citations

Abstract

Abstract A new type of alkyne esterification was developed under electrochemical conditions using alkyne aldehydes and alcohol compounds as starting materials and carbene and iodine as mediators. Through this method, external oxidants and transition metals are excluded and the alkyne bond is fully preserved. This approach is compatible with a wide range of substrates and various functional groups and provides a green and mild new route for directly converting alkyne aldehydes into alkyne esters.

ChemCatChemVol. 17(3)
Guangxi Normal University (CN)
National Natural Science Foundation of China
Clean water and sanitation
Openalex Percentile: Top 47%
Oxidative Organic Chemistry Reactions
0.25
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