Visible-Light-Induced Cascade Cyclization of Isocyanobiaryls with Hydrosilanes for the Synthesis of 6-Silylated Phenanthridines

A visible-light-induced cascade cyclization of isocyanobiaryls with hydrosilanes has been developed for the synthesis of 6-silylated phenanthridines. Readily available hydrosilanes were employed as silyl radical precursors under room-temperature conditions. The merits of the transformation include operational simplicity, mild conditions, high atom economy, and good functional group compatibility.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-09-09
DOI
https://doi.org/10.1021/acs.joc.5c01891
Citations
2
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
1.87
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article

Visible-Light-Induced Cascade Cyclization of Isocyanobiaryls with Hydrosilanes for the Synthesis of 6-Silylated Phenanthridines

Yanqi Li, Heyun Sheng, Yanping Li, Yongqi Yu et al.
2 citations
The Journal of Organic Chemistry
Radical Photochemical Reactions
1.87
article

Visible-Light-Induced Cascade Cyclization of Isocyanobiaryls with Hydrosilanes for the Synthesis of 6-Silylated Phenanthridines

Yanqi Li, Heyun Sheng, Yanping Li, Yongqi Yu, Weiguang Kong, Ting Li, Ming Chen, Wenguang Li, Mengdan You
article en
2 citations

Abstract

A visible-light-induced cascade cyclization of isocyanobiaryls with hydrosilanes has been developed for the synthesis of 6-silylated phenanthridines. Readily available hydrosilanes were employed as silyl radical precursors under room-temperature conditions. The merits of the transformation include operational simplicity, mild conditions, high atom economy, and good functional group compatibility.

The Journal of Organic ChemistryVol. 90(37)
Nanyang Normal University (CN), Pharmaceutical Biotechnology (Czechia) (CZ)
Openalex Percentile: Top 14%
Radical Photochemical Reactions
1.87
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