“…The bioorthogonal reactivity of these aldehyde sites generated by UDG has been previously exploited for site-selective attachment of oxyamine, hydrazine, or hydrazide-based chemical probes for biological and biomedical applications. However, this strategy has not been explored for attachment of catalysts. − Notably, both dU-containing DNA and E. coli UDG are cheaply and widely available, potentially allowing systematic investigations into the DNA sequence effect on reaction outcomes in a high-throughput format as well as permitting site-specific modification of long and complex DNA scaffolds which are otherwise challenging using phosphoramidite chemistry.…”