| Literature DB >> 30615417 |
Eduardo de Pedro Beato1, Julián Priego1, Adrián Gironda-Martínez1, Fernando González1, Jesús Benavides1, Jesús Blas1, María Dolores Martín-Ortega1, Miguel Ángel Toledo1, Jesús Ezquerra1, Alicia Torrado1.
Abstract
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.Entities:
Keywords: C−N bond formation; DNA-encoded chemical libraries
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Year: 2019 PMID: 30615417 DOI: 10.1021/acscombsci.8b00142
Source DB: PubMed Journal: ACS Comb Sci ISSN: 2156-8944 Impact factor: 3.784