Litcius/Paper detail

Aryl diazonium intermediates enable mild DNA-compatible C–C bond formation for medicinally relevant combinatorial library synthesis

Xianfeng Li, Juan Zhang, Changyang Liu, Jie Sun, Yangfeng Li, Yangfeng Li, Gong Zhang, Yizhou Li, Yizhou Li

2022Chemical Science28 citationsDOIOpen Access PDF

Abstract

, hydroxamic acid), emphasizing the superiority of the aryl diazonium-based approach. Together with the convenient transformation into an aryl azide photo-crosslinker, aryl diazonium's DNA-compatible diversification synergistically demonstrated its competence to create medicinally relevant combinatorial libraries and investigate protein-ligand interactions in pharmaceutical research.

Topics & Concepts

ArylCombinatorial chemistrySubstrate (aquarium)Functional groupHalideChemistryOrthogonalityScope (computer science)Organic chemistryComputer scienceBiologyMathematicsProgramming languagePolymerAlkylGeometryEcologyChemical Synthesis and AnalysisClick Chemistry and ApplicationsSynthesis and Biological Evaluation