Methionine-facilitated chalcogenation of peptides through palladium-catalyzed β-C(sp<sup>3</sup>)–H activation

We report a novel methodology for the site-selective chalcogenation of peptides <i>via</i> Pd-catalyzed β-C(sp<sup>3</sup>)-H activation. In this study, native methionine residues serve as an intrinsic directing group, while various diaryl disulfides/diselenides act as coupling partners, affording chalcogenated peptides in moderate to good isolated yields.

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Publication Details

Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc04285b
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94
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article

Methionine-facilitated chalcogenation of peptides through palladium-catalyzed β-C(sp3)–H activation

Yi Sun, Fengjie Lu, Yuqi Pan, Qi Lu et al.
1 citations
Chemical Communications
Catalytic C–H Functionalization Methods
0.94
article

Methionine-facilitated chalcogenation of peptides through palladium-catalyzed β-C(sp3)–H activation

Yi Sun, Fengjie Lu, Yuqi Pan, Qi Lu, Wei Qu
article en
1 citations

Abstract

We report a novel methodology for the site-selective chalcogenation of peptides <i>via</i> Pd-catalyzed β-C(sp<sup>3</sup>)-H activation. In this study, native methionine residues serve as an intrinsic directing group, while various diaryl disulfides/diselenides act as coupling partners, affording chalcogenated peptides in moderate to good isolated yields.

Chemical CommunicationsVol. 61(85)
Qufu Normal University (CN)
Openalex Percentile: Top 21%
Catalytic C–H Functionalization Methods
0.94
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