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• W2622019389 abstract "An irreversible, three-component assembly with 2-formylphenylboronic acid, catechol, and N-hydroxylamines was achieved in aqueous media. The boronate ester product was formed with substituted catechols including l-DOPA. Assembly was found to be orthogonal to common biological functional groups and both copper(I)-catalyzed alkyne-azide cycloaddition and aminoether/carbonyl condensations. Boronate ester formation and aminoether condensation were achieved in one pot with a hexameric peptide." @default.
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• W2622019389 date "2017-06-05" @default.
• W2622019389 modified "2023-09-27" @default.
• W2622019389 title "Boronic Acid Mediated Coupling of Catechols and <i>N</i>-Hydroxylamines: A Bioorthogonal Reaction to Label Peptides" @default.
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• W2622019389 doi "https://doi.org/10.1021/acs.orglett.7b01198" @default.
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