Visible-light-promoted azidation/arylation of unactivated alkenes with Togni-N<sub>3</sub><i>via</i> electron donor–acceptor complexes

A visible-light-promoted azidation/arylation of unactivated alkenes with Togni-N<sub>3</sub> has been achieved, leading to a series of azidated pyrrolo[1,2-<i>a</i>]indoles under photocatalyst-free conditions. Notably, an EDA complex derived from the electron-rich indole derivatives and Togni-N<sub>3</sub> served as the key intermediate in this reaction.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2024-12-30
DOI
https://doi.org/10.1039/d4ob01861c
Citations
3
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.75

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article

Visible-light-promoted azidation/arylation of unactivated alkenes with Togni-N3via electron donor–acceptor complexes

Chenqi Wu, Peidong Cheng, Yong Zhang, Peng Xie et al.
3 citations
Organic & Biomolecular Chemistry
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article

Visible-light-promoted azidation/arylation of unactivated alkenes with Togni-N3via electron donor–acceptor complexes

Chenqi Wu, Peidong Cheng, Yong Zhang, Peng Xie, Song Sun, Yue Gao
article en
3 citations

Abstract

A visible-light-promoted azidation/arylation of unactivated alkenes with Togni-N<sub>3</sub> has been achieved, leading to a series of azidated pyrrolo[1,2-<i>a</i>]indoles under photocatalyst-free conditions. Notably, an EDA complex derived from the electron-rich indole derivatives and Togni-N<sub>3</sub> served as the key intermediate in this reaction.

Organic & Biomolecular ChemistryVol. 23(7)
Suzhou Polytechnic Institute of Agriculture (CN), Changzhou University (CN), Suzhou Industrial Park Institute of Services Outsourcing (CN)
Qinglan Project of Jiangsu Province of China
Openalex Percentile: Top 30%
Radical Photochemical Reactions
0.75
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