Transient Directing Group-Assisted Palladium-Catalyzed C4-Alkynylation of Indoles

Pd-catalyzed C4-selective alkynylation of indoles was established by employing glycine as a transient directing group. This reaction exhibits high regioselectivity with the tolerance of a wide scope of functional groups to afford diverse alkynylated indoles in moderate to good yields. Moreover, the readily accessible scale-up synthesis and further decorations to achieve multifunctionalized indoles demonstrate the synthetic potential of this protocol.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-01-10
DOI
https://doi.org/10.1021/acs.joc.4c02478
Citations
4
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
3.74

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article

Transient Directing Group-Assisted Palladium-Catalyzed C4-Alkynylation of Indoles

Wanqing Wu, Huanfeng Jiang, Shuqi Guo, Shaorong Yang
4 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
3.74
article

Transient Directing Group-Assisted Palladium-Catalyzed C4-Alkynylation of Indoles

Wanqing Wu, Huanfeng Jiang, Shuqi Guo, Shaorong Yang
article en
4 citations

Abstract

Pd-catalyzed C4-selective alkynylation of indoles was established by employing glycine as a transient directing group. This reaction exhibits high regioselectivity with the tolerance of a wide scope of functional groups to afford diverse alkynylated indoles in moderate to good yields. Moreover, the readily accessible scale-up synthesis and further decorations to achieve multifunctionalized indoles demonstrate the synthetic potential of this protocol.

The Journal of Organic ChemistryVol. 90(3)
South China University of Technology (CN)
Guangzhou Municipal Science and Technology Project, Basic and Applied Basic Research Foundation of Guangdong Province
Zero hunger
Openalex Percentile: Top 9%
Catalytic C–H Functionalization Methods
3.74
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