Cover Feature: Overriding Cage Effect in Electron Donor‐Acceptor Photoactivation of Diaryliodonium Reagents: Synthesis of Chalcogenides (Chem. Eur. J. 61/2024)

An electron donor–acceptor photoactivation platform of diaryliodonium reagents has been developed, in which generated aryl radicals override the cage effect to get captured by dichalcogenides en route to the synthesis of a wide variety of di(hetero)aryl and aryl–alkyl chalcogenides. The chalcogenation technology applies to late-stage functionalizations and disulfide bioconjugations, and facilitates access to bioactive compounds and pharmaceuticals. More information can be found in the Research Article by L. Roy, S. Murarka and co-workers (DOI: 10.1002/chem.202402969).

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Publication Details

Journal
Chemistry - A European Journal
Published
2024-11-04
DOI
https://doi.org/10.1002/chem.202486104
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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Cover Feature: Overriding Cage Effect in Electron Donor‐Acceptor Photoactivation of Diaryliodonium Reagents: Synthesis of Chalcogenides (Chem. Eur. J. 61/2024)

Prahallad Meher, Sushanta Kumar Parida, Sandip Murarka, Lisa Roy et al.
Chemistry - A European Journal
Sulfur-Based Synthesis Techniques
article

Cover Feature: Overriding Cage Effect in Electron Donor‐Acceptor Photoactivation of Diaryliodonium Reagents: Synthesis of Chalcogenides (Chem. Eur. J. 61/2024)

Prahallad Meher, Sushanta Kumar Parida, Sandip Murarka, Lisa Roy, Sanat Kumar Mahapatra
article en

Abstract

An electron donor–acceptor photoactivation platform of diaryliodonium reagents has been developed, in which generated aryl radicals override the cage effect to get captured by dichalcogenides en route to the synthesis of a wide variety of di(hetero)aryl and aryl–alkyl chalcogenides. The chalcogenation technology applies to late-stage functionalizations and disulfide bioconjugations, and facilitates access to bioactive compounds and pharmaceuticals. More information can be found in the Research Article by L. Roy, S. Murarka and co-workers (DOI: 10.1002/chem.202402969).

Chemistry - A European JournalVol. 30(61)
Indian Institute of Technology Jodhpur (IN), Institute of Chemical Technology (IN), Indian Institute of Technology Bhubaneswar (IN)
Clean water and sanitation
Openalex Percentile: Top 86%
Sulfur-Based Synthesis Techniques
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Cover Feature: Overriding Cage Effect in Electron Donor‐Acceptor Photoactivation of Diaryliodonium Reagents: Synthesis of Chalcogenides (Chem. Eur. J. 61/2024) — Prahallad Meher, Sushanta Kumar Parida, et al. · Chemistry - A European Journal (2024) | TGRS Research Map | TGRS