Solvent-Dependent Chemoselectivity Switch to Arg-Lys Imidazole Cross-Links

Herein, we report a trifluoroethanol-mediated, chemoselective method for the formation of Arg-Lys imidazole cross-links with methylglyoxal and its application in the selective macrocyclization of peptides between Lys and Arg and the late-stage diversification of Lys-containing peptides with guanidine. Our findings highlight the critical role of solvent choice in controlling chemoselectivity, providing valuable insights into solvent-dependent peptide modification.

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Publication Details

Journal
Organic Letters
Published
2024-09-20
DOI
https://doi.org/10.1021/acs.orglett.4c03101
Citations
5
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
1.25

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article

Solvent-Dependent Chemoselectivity Switch to Arg-Lys Imidazole Cross-Links

Monika Raj, Ana Villalobos Galindo
5 citations
Organic Letters
Click Chemistry and Applications
1.25
article

Solvent-Dependent Chemoselectivity Switch to Arg-Lys Imidazole Cross-Links

Monika Raj, Ana Villalobos Galindo
article en
5 citations

Abstract

Herein, we report a trifluoroethanol-mediated, chemoselective method for the formation of Arg-Lys imidazole cross-links with methylglyoxal and its application in the selective macrocyclization of peptides between Lys and Arg and the late-stage diversification of Lys-containing peptides with guanidine. Our findings highlight the critical role of solvent choice in controlling chemoselectivity, providing valuable insights into solvent-dependent peptide modification.

Organic LettersVol. 26(39)
Emory University (US)
American Cancer Society, National Human Genome Research Institute
Openalex Percentile: Top 22%
Click Chemistry and Applications
1.25
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