Selective <i>C‐Meth</i>ylenation of <i>N</i>‐Unsubstituted Indoles Using CO<sub>2</sub> Under NaBH<sub>4</sub>/I<sub>2</sub> System

The selective C-methylenation of N-unsubstituted indoles using CO<sub>2</sub> as the C1 source to access diindolylmethane (DIM) and its derivatives is described. This reaction provides a novel method for four-electron reductive functionalization of CO<sub>2</sub> with N-unsubstituted indoles via formation of C-CH<sub>2</sub>-C bonds, and a new access to molecular structures.

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Publication Details

Journal
ChemSusChem
Published
2024-08-26
DOI
https://doi.org/10.1002/cssc.202401491
Citations
2
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.32

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article

Selective C‐Methylenation of N‐Unsubstituted Indoles Using CO2 Under NaBH4/I2 System

Zhiqiang Guo, Chanjuan Xi, Jinglong Wu, Xue-Hong Wei
2 citations
ChemSusChem
Asymmetric Hydrogenation and Catalysis
0.32
article

Selective C‐Methylenation of N‐Unsubstituted Indoles Using CO2 Under NaBH4/I2 System

Zhiqiang Guo, Chanjuan Xi, Jinglong Wu, Xue-Hong Wei
article en
2 citations

Abstract

The selective C-methylenation of N-unsubstituted indoles using CO<sub>2</sub> as the C1 source to access diindolylmethane (DIM) and its derivatives is described. This reaction provides a novel method for four-electron reductive functionalization of CO<sub>2</sub> with N-unsubstituted indoles via formation of C-CH<sub>2</sub>-C bonds, and a new access to molecular structures.

ChemSusChemVol. 18(2)
Shanxi University (CN), Tsinghua University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Shanxi Province
Openalex Percentile: Top 50%
Asymmetric Hydrogenation and Catalysis
0.32
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