Chemo-SelectiveElectrochemical Pinacol Coupling ofAldehydes and Ketones Using TMSN<sub>3</sub> as a Promoter

The pinacol coupling is a significant method for carbon–carbon bond formation. Here, we present an efficient electrochemical approach for pinacol coupling of aldehydes and ketones using TMSN<sub>3</sub> as a sacrificial reagent. This method exhibits broad applicability to aryl, heteroaryl, and alkyl aldehydes/ketones with excellent chemo-selectivity and high yields (40 examples, up to 99% yield) under mild conditions. This method can also be applied in the selective reduction of phthalimides to hydroxyl lactams in good yields. The proposed mechanism was elucidated by control experiments and cyclic voltammetry.

Publication Details

Journal
Figshare
Published
2025-02-04
DOI
https://doi.org/10.1021/acs.joc.4c02147.s001
Primary Topic
Radical Photochemical Reactions
Type
article
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Chemo-SelectiveElectrochemical Pinacol Coupling ofAldehydes and Ketones Using TMSN3 as a Promoter

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Radical Photochemical Reactions
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Chemo-SelectiveElectrochemical Pinacol Coupling ofAldehydes and Ketones Using TMSN3 as a Promoter

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Abstract

The pinacol coupling is a significant method for carbon–carbon bond formation. Here, we present an efficient electrochemical approach for pinacol coupling of aldehydes and ketones using TMSN<sub>3</sub> as a sacrificial reagent. This method exhibits broad applicability to aryl, heteroaryl, and alkyl aldehydes/ketones with excellent chemo-selectivity and high yields (40 examples, up to 99% yield) under mild conditions. This method can also be applied in the selective reduction of phthalimides to hydroxyl lactams in good yields. The proposed mechanism was elucidated by control experiments and cyclic voltammetry.

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Radical Photochemical Reactions
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Chemo-SelectiveElectrochemical Pinacol Coupling ofAldehydes and Ketones Using TMSN<sub>3</sub> as a Promoter · Figshare (2025) | TGRS Research Map | TGRS