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Palladium-Mediated Hydroamination of DNA-Conjugated Aryl Alkenes

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C-N bond formation is one of the most commonly used reactions in medicinal chemistry. Herein, we report an efficient Pd-promoted hydroamination reaction between DNA-conjugated aryl alkenes and a wide scope… Click to show full abstract

C-N bond formation is one of the most commonly used reactions in medicinal chemistry. Herein, we report an efficient Pd-promoted hydroamination reaction between DNA-conjugated aryl alkenes and a wide scope of aliphatic amines. The described reactions are demonstrated in good to excellent conversions to furnish C (sp3)–N bonds on DNA. This DNA-compatible transformation has strong potentials for the application into DNA-encoded library synthesis.

Keywords: dna; dna conjugated; chemistry; hydroamination; aryl alkenes; conjugated aryl

Journal Title: Frontiers in Chemistry
Year Published: 2022

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