Abstract
Conversion of amines into azides using imidazole-1-sulfonyl azide as a diazotransfer reagent has proven to be a straightforward way to introduce targetable handles into proteins. We explored whether less toxic and milder conditions than described before could be applied. It was shown that the aqueous diazotransfer proceeds without adding Cu(II) not only at pH 11 but also at pH 8.5. The diazotransfer was shown to be selective towards a single amine.
Original language | English |
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Pages (from-to) | 701-705 |
Number of pages | 5 |
Journal | Chemical Science |
Volume | 2 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2011 |
Bibliographical note
Copyright:Copyright 2011 Elsevier B.V., All rights reserved.