Electrochemical C3‐Site‐Selective Cyanation of Substituted Indoles

ABSTRACT An electrochemical strategy for C3‐site selective cyanation of substituted indoles is reported. This protocol employs TMSCN as a cyano source, yielding C3‐cyano indoles in moderate to good yields. The electrochemical strategy is distinguished by its mild and oxidant‐free conditions, with good regioselectivity. A variety of protected and unprotected indoles has been successfully utilized in this methodology.

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Journal
ChemistrySelect
Published
2026-05-01
DOI
https://doi.org/10.1002/slct.202600055
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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0.00
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article

Electrochemical C3‐Site‐Selective Cyanation of Substituted Indoles

Jaswant Kumar, Sasikumar Kuttappan, Paranjay Parikh, Gajendrasinh Raolji et al.
ChemistrySelect
Catalytic C–H Functionalization Methods
article

Electrochemical C3‐Site‐Selective Cyanation of Substituted Indoles

Jaswant Kumar, Sasikumar Kuttappan, Paranjay Parikh, Gajendrasinh Raolji, Saurabh Vijay
article en

Abstract

ABSTRACT An electrochemical strategy for C3‐site selective cyanation of substituted indoles is reported. This protocol employs TMSCN as a cyano source, yielding C3‐cyano indoles in moderate to good yields. The electrochemical strategy is distinguished by its mild and oxidant‐free conditions, with good regioselectivity. A variety of protected and unprotected indoles has been successfully utilized in this methodology.

ChemistrySelectVol. 11(17)
Piramal (India) (IN)
Openalex Percentile: Top 11%
Catalytic C–H Functionalization Methods
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