Ag( <scp>i</scp> )-mediated <i>mono</i> -selective C(sp <sup>2</sup> )–H chalcogenation of α-aminotropones and their peptides at room temperature

This report describes an Ag(I)-mediated strategy for the <i>mono</i>-selective chalcogenation of α-aminotropones and their peptides with a range of disulfides and diselenides at ambient temperature. The method efficiently furnishes <i>mono</i>-chalcogenated aminotropone derivatives in moderate to good yields, while demonstrating compatibility with diverse substrates and functional groups, offering synthetic versatility in downstream applications.

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Publication Details

Journal
Chemical Communications
Published
2025-12-01
DOI
https://doi.org/10.1039/d5cc05556c
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.94

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article

Ag( i )-mediated mono -selective C(sp 2 )–H chalcogenation of α-aminotropones and their peptides at room temperature

Nagendra K. Sharma, Malobika Kar
1 citations
Chemical Communications
Sulfur-Based Synthesis Techniques
0.94
article

Ag( i )-mediated mono -selective C(sp 2 )–H chalcogenation of α-aminotropones and their peptides at room temperature

Nagendra K. Sharma, Malobika Kar
article en
1 citations

Abstract

This report describes an Ag(I)-mediated strategy for the <i>mono</i>-selective chalcogenation of α-aminotropones and their peptides with a range of disulfides and diselenides at ambient temperature. The method efficiently furnishes <i>mono</i>-chalcogenated aminotropone derivatives in moderate to good yields, while demonstrating compatibility with diverse substrates and functional groups, offering synthetic versatility in downstream applications.

Chemical CommunicationsVol. 62(2)
National Institute of Science Education and Research (IN), Homi Bhabha National Institute (IN)
National Institute of Science Education and Research, Science and Engineering Research Board
Openalex Percentile: Top 19%
Sulfur-Based Synthesis Techniques
0.94
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