Electrochemical Synthesis of Ketones via Metal-Free Decarboxylative Coupling of Vinyl Azides and NHPI Esters

Abstract We introduce a metal-free method for C–C bond formation by coupling NHPI esters with vinyl azides through electrochemical synthesis. By converting carboxylic acids into radical-initiating NHPI esters, our approach achieves efficient C(sp³)–C(sp3) bond formation without needing metal catalysts. This method is highly adaptable, enabling the coupling of various NHPI esters with a broad range of vinyl azides, including those with halide or heteroatom substitutions.

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Publication Details

Journal
Synlett
Published
2025-05-14
DOI
https://doi.org/10.1055/a-2608-2142
Citations
1
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.94

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article

Electrochemical Synthesis of Ketones via Metal-Free Decarboxylative Coupling of Vinyl Azides and NHPI Esters

Satpal Singh Badsara, Siddharth Sharma
1 citations
Synlett
Radical Photochemical Reactions
0.94
article

Electrochemical Synthesis of Ketones via Metal-Free Decarboxylative Coupling of Vinyl Azides and NHPI Esters

Satpal Singh Badsara, Siddharth Sharma
article en
1 citations

Abstract

Abstract We introduce a metal-free method for C–C bond formation by coupling NHPI esters with vinyl azides through electrochemical synthesis. By converting carboxylic acids into radical-initiating NHPI esters, our approach achieves efficient C(sp³)–C(sp3) bond formation without needing metal catalysts. This method is highly adaptable, enabling the coupling of various NHPI esters with a broad range of vinyl azides, including those with halide or heteroatom substitutions.

SynlettVol. 36(15)
Mohanlal Sukhadia University (IN), Banaras Hindu University (IN)
Banaras Hindu University, Science and Engineering Research Board, Rashtriya Uchchatar Shiksha Abhiyan
Openalex Percentile: Top 26%
Radical Photochemical Reactions
0.94
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