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• W3048696568 abstract "Abstract Se‐benzyl selenoimidazolium salts are characterized by remarkable alkyl‐transfer potential under physiological conditions. Structure‐activity relationship studies show that selective monoalkylation of primary amines depends on supramolecular interactions between the selenoimidazole leaving group and the target nucleophile. We demonstrate that these reagents can be used for site‐selective and nearly quantitative modification of the model protein lysozyme on Lys13, bypassing the higher intrinsic reactivities of Lys1 and Lys33. These observations introduce selenoimidazolium salts as novel class of electrophiles for selective N‐alkylation of native proteins." @default.
• W3048696568 created "2020-08-18" @default.
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• W3048696568 date "2020-09-18" @default.
• W3048696568 modified "2023-10-18" @default.
• W3048696568 title "Selenoimidazolium Salts as Supramolecular Reagents for Protein Alkylation" @default.
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• W3048696568 doi "https://doi.org/10.1002/cbic.202000557" @default.
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• W3048696568 hasPublicationYear "2020" @default.
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