Silver‐Catalyzed Halochalcogenation of Terminal Alkynols to Access Halogenated Selenonaphthalenes

Herein, we report an AgNO<sub>3</sub> and FeCl<sub>3</sub> relay-catalyzed halogenation and electrophilic selenium cyclization reaction. This reaction is based on the trifunctionalization of terminal alkynols using NBS and diorganyl diselenides, providing a step-efficient synthetic approach to produce halogenated selenonaphthalene derivatives in good yields. Furthermore, the halochalcogenation and cyclization reaction offers an efficient protocol for constructing molecules with two independent reactive centers.

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Publication Details

Journal
Chemistry - A European Journal
Published
2025-03-22
DOI
https://doi.org/10.1002/chem.202500683
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.94
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article

Silver‐Catalyzed Halochalcogenation of Terminal Alkynols to Access Halogenated Selenonaphthalenes

Yibiao Li, Huanliang Hong, Sijie Xie, Li Wang
1 citations
Chemistry - A European Journal
Sulfur-Based Synthesis Techniques
0.94
article

Silver‐Catalyzed Halochalcogenation of Terminal Alkynols to Access Halogenated Selenonaphthalenes

Yibiao Li, Huanliang Hong, Sijie Xie, Li Wang
article en
1 citations

Abstract

Herein, we report an AgNO<sub>3</sub> and FeCl<sub>3</sub> relay-catalyzed halogenation and electrophilic selenium cyclization reaction. This reaction is based on the trifunctionalization of terminal alkynols using NBS and diorganyl diselenides, providing a step-efficient synthetic approach to produce halogenated selenonaphthalene derivatives in good yields. Furthermore, the halochalcogenation and cyclization reaction offers an efficient protocol for constructing molecules with two independent reactive centers.

Chemistry - A European JournalVol. 31(25)
Wuyi University (CN), Wuyi University (CN)
Openalex Percentile: Top 28%
Sulfur-Based Synthesis Techniques
0.94
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