Visible-light-mediated synthesis of 2-sulfenylated pyrrolo[1,2-α]quinoxalines <i>via</i> isocyanide/disulfide radical cascades

We have developed a visible-light-driven photocatalytic tandem reaction system to achieve the efficient synthesis of 2-sulfenylated pyrrolo[1,2-α]quinoxalines based on a radical addition-cyclization mechanism. Mechanistic studies show that the sulfur radical intermediates generated in the reaction system directly participate in the subsequent formation of C-S bonds. This strategy has opened up an efficient synthetic pathway for the precise synthesis of C2-sulfur-substituted heterocyclic compounds.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob00451a
Citations
2
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
1.87

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article

Visible-light-mediated synthesis of 2-sulfenylated pyrrolo[1,2-α]quinoxalines via isocyanide/disulfide radical cascades

Pei‐Qing Zheng, Songzhi Kong, Xia Luo, Haisheng Xie et al.
2 citations
Organic & Biomolecular Chemistry
Sulfur-Based Synthesis Techniques
1.87
article

Visible-light-mediated synthesis of 2-sulfenylated pyrrolo[1,2-α]quinoxalines via isocyanide/disulfide radical cascades

Pei‐Qing Zheng, Songzhi Kong, Xia Luo, Haisheng Xie, Xiai Luo, Mengqiang Wu, Chen Chen, yazi Deng
article en
2 citations

Abstract

We have developed a visible-light-driven photocatalytic tandem reaction system to achieve the efficient synthesis of 2-sulfenylated pyrrolo[1,2-α]quinoxalines based on a radical addition-cyclization mechanism. Mechanistic studies show that the sulfur radical intermediates generated in the reaction system directly participate in the subsequent formation of C-S bonds. This strategy has opened up an efficient synthetic pathway for the precise synthesis of C2-sulfur-substituted heterocyclic compounds.

Organic & Biomolecular ChemistryVol. 23(24)
Hunan University of Traditional Chinese Medicine (CN), Guangdong Ocean University (CN)
Guangdong Ocean University
Openalex Percentile: Top 15%
Sulfur-Based Synthesis Techniques
1.87
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