Matthias Krumb; Lisa Marie Kammer; Shorouk O. Badir; María Jesús Cabrera-Afonso; Victoria E. Wu; Minxue Huang; Adam Csakai; Lisa A. Marcaurelle; Gary A Molander
Chem. Sci., 2022, 13, 1023-1029
https://doi.org/10.1039/D1SC05683B

Abstract

DNA-encoded library (DEL) technology has emerged as a time- and cost-efficient technique for the identification of therapeutic candidates in the pharmaceutical industry. Although several reaction classes have been successfully validated in DEL environments, there remains a paucity of DNA-compatible reactions that harness building blocks (BBs) from readily available substructures bearing multifunctional handles for further library diversification under mild, dilute, and aqueous conditions. In this study, the direct C–H carbofunctionalization of medicinally-relevant heteroarenes can be accomplished via the photoreduction of DNA-conjugated (hetero)aryl halides to deliver reactive aryl radical intermediates in a regulated fashion within minutes of blue light illumination. A broad array of electron-rich and electron-poor heteroarene scaffolds undergo transformation in the presence of sensitive functional groups.