"Photoclick" postsynthetic modification of DNA
- Angew Chem Int Ed Engl. 2014 Dec 22;53(52):14580-2. doi: 10.1002/anie.201407874.
- 1. Institute of Organic Chemistry, Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 6, 76131 Karlsruhe (Germany).
A new DNA building block bearing a push-pull-substituted diaryltetrazole linked to the 5-position of 2'-deoxyuridine through an aminopropynyl group was synthesized. The accordingly modified oligonucleotide allows postsynthetic labeling with a maleimide-modified sulfo-Cy3 dye, N-methylmaleimide, and methylmethacrylate as dipolarophiles by irradiation at 365 nm (LED). The determined rate constant of (23±7) M(-1) s(-1) is remarkably high with respect to Other copper-free bioorthogonal reactions and comparable with the copper-catalyzed cycloaddition between azides and acetylenes.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: Fluorescent DyeResearch Areas: Others