| Literature DB >> 27619479 |
Brandon M Cornali1, Flora W Kimani1, John C Jewett1.
Abstract
Triazabutadienes can be used to readily generate reactive aryl diazonium ions under mild, physiologically relevant conditions. These conditions are compatible with a range of functionalities that do not tolerate traditional aryl diazonium ion generation. To increase the utility of this aryl diazonium ion releasing chemistry an alkyne-containing triazabutadiene was synthesized. The copper-catalyzed azide-alkyne cycloaddition ("Cu-click") reaction was utilized to modify the alkyne-containing triazabutadiene and shown to be compatible with the nitrogen-rich triazabutadiene. One of the triazole products was tethered to a fluorophore, thus enabling the direct fluorescent labeling of a model protein.Entities:
Year: 2016 PMID: 27619479 DOI: 10.1021/acs.orglett.6b02420
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005