DNA-encoded library technology (ELT) has emerged in the pharmaceutical industry as a powerful tool for hit and lead generation. Over the last 10 years, a number of DNA-compatible chemical reactions have been published and used to synthesize libraries. Among the most commonly used reactions in medicinal chemistry is the C−N bond formation, and its application to DNA-encoded library technology affords an alternative approach to identify high-affinity binders for biologically relevant protein targets. Herein we report a newly developed Pd-promoted C−N cross coupling reaction between DNA-conjugated aryl bromides and a wide scope of arylamines in good to excellent yields. The mild reaction conditions should facilitate the synthesis of novel DNA-encoded combinatorial libraries.

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Eight different biodegradable chitosan‐supported bifunctional chiral thioureas have been prepared as a greener and more sustainable alternative to those supported on petrochemical‐derived polymers. These organocatalysts promoted an enantioselective aza‐Henry reaction, which afforded good product yields with moderate to high enantioselectivity. The activity and stereodirecting ability of these materials were dependent on the accessibility of the reactants to the active site and increased with the length of the tether that connected the thiourea to the biopolymer. The best performing catalyst was able to be recovered and recycled five times without a loss of activity.

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