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• W2519283548 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." @default.
• W2519283548 created "2016-09-23" @default.
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• W2519283548 date "2016-09-13" @default.
• W2519283548 modified "2023-10-14" @default.
• W2519283548 title "Cu-Click Compatible Triazabutadienes To Expand the Scope of Aryl Diazonium Ion Chemistry" @default.
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• W2519283548 doi "https://doi.org/10.1021/acs.orglett.6b02420" @default.
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