Direct and Site-Selective C–H Cyanation of (Hetero)arenes by a Nontoxic Cyano Source

Direct C-H cyanation of arenes and heteroarenes is herein reported using a nontoxic cyano source with high regioselectivity. CuI serves as an essential multifunctional catalyst, which promotes the in situ generation of Cu-CN and aryl iodides and the subsequent cross-coupling of these two intermediates to yield aryl nitrile products. The new strategy of C-H cyanation, good regioselectivity, and the use of a nontoxic cyano source together represents a significant advancement in cyanation chemistry.

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Publication Details

Journal
Organic Letters
Published
2025-06-19
DOI
https://doi.org/10.1021/acs.orglett.5c01963
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.87

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article

Direct and Site-Selective C–H Cyanation of (Hetero)arenes by a Nontoxic Cyano Source

Songlin Zhang, Ao Xu
2 citations
Organic Letters
Catalytic C–H Functionalization Methods
1.87
article

Direct and Site-Selective C–H Cyanation of (Hetero)arenes by a Nontoxic Cyano Source

Songlin Zhang, Ao Xu
article en
2 citations

Abstract

Direct C-H cyanation of arenes and heteroarenes is herein reported using a nontoxic cyano source with high regioselectivity. CuI serves as an essential multifunctional catalyst, which promotes the in situ generation of Cu-CN and aryl iodides and the subsequent cross-coupling of these two intermediates to yield aryl nitrile products. The new strategy of C-H cyanation, good regioselectivity, and the use of a nontoxic cyano source together represents a significant advancement in cyanation chemistry.

Organic LettersVol. 27(26)
Jiangnan University (CN), Ministry of Education of the People's Republic of China (CN)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 15%
Catalytic C–H Functionalization Methods
1.87
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