Ag(I)-Mediated Site-Selective C(sp<sup>2</sup>)-H Chalcogenation of Tryptophan-Peptides with Dichalcogenides at Room Temperature

This report presents a silver-mediated site-selective chalcogenation of tryptophan-containing peptides with various dichalcogenides (disulfides/diselenides) at room temperature in good to excellent yields. The significant features include broad substrate scope, functional group diversity, late-stage modification of drug molecules (Dopamine and Levodopa), and various valuable postsynthetic transformations under mild conditions.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-10-07
DOI
https://doi.org/10.1021/acs.joc.4c01730
Citations
8
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
2.00

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article

Ag(I)-Mediated Site-Selective C(sp2)-H Chalcogenation of Tryptophan-Peptides with Dichalcogenides at Room Temperature

Raghunath Bag, Nagendra K. Sharma, Malobika Kar
8 citations
The Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
2.00
article

Ag(I)-Mediated Site-Selective C(sp2)-H Chalcogenation of Tryptophan-Peptides with Dichalcogenides at Room Temperature

Raghunath Bag, Nagendra K. Sharma, Malobika Kar
article en
8 citations

Abstract

This report presents a silver-mediated site-selective chalcogenation of tryptophan-containing peptides with various dichalcogenides (disulfides/diselenides) at room temperature in good to excellent yields. The significant features include broad substrate scope, functional group diversity, late-stage modification of drug molecules (Dopamine and Levodopa), and various valuable postsynthetic transformations under mild conditions.

The Journal of Organic ChemistryVol. 89(20)
National Institute of Science Education and Research (IN), Homi Bhabha National Institute (IN)
Department of Atomic Energy, Government of India, Science and Engineering Research Board
Openalex Percentile: Top 14%
Sulfur-Based Synthesis Techniques
2.00
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