Publication | Open Access
Screening of Three Transition Metal‐Mediated Reactions Compatible with DNA‐Encoded Chemical Libraries
52
Citations
41
References
2019
Year
Combinatorial ChemistryBioorganic ChemistryEngineeringMolecular BiologyOrganic ChemistryChemistrySuzuki Cross-couplingChemical BiologyNucleic Acid ChemistryBioorganometallic ChemistryDna-encoded Chemical LibrariesOrganometallic CatalysisCross-coupling ReactionOligonucleotideCatalysisAsymmetric CatalysisDna‐encoded Chemical LibrariesBiomolecular EngineeringSonogashira Cross-couplingNatural Sciences
The construction of DNA-encoded chemical libraries (DECLs) crucially relies on the availability of chemical reactions, which are DNA-compatible and which exhibit high conversion rates for a large number of diverse substrates. In this work, we present our optimization and validation procedures for three copper and palladium-catalyzed reactions (Suzuki cross-coupling, Sonogashira cross-coupling and copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC)), which have been successfully used by our group for the construction of large encoded libraries.
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