Development of a Micellar-Promoted Heck Reaction for the Synthesis of DNA-Encoded Libraries

The capability of DNA encoded libraries (DELs) as a method of small molecule hit identification is becoming widely established in drug discovery. While their selection method offers advantages over more traditional means, DELs are limited by the chemistry that can be utilized to construct them. Sign...

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Veröffentlicht in:Bioconjugate chemistry 2023-03, Vol.34 (4), p.756-763
Hauptverfasser: Stanway-Gordon, Harriet A., Odger, Jake A., Waring, Michael J.
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container_issue 4
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container_title Bioconjugate chemistry
container_volume 34
creator Stanway-Gordon, Harriet A.
Odger, Jake A.
Waring, Michael J.
description The capability of DNA encoded libraries (DELs) as a method of small molecule hit identification is becoming widely established in drug discovery. While their selection method offers advantages over more traditional means, DELs are limited by the chemistry that can be utilized to construct them. Significant advances in DNA compatible chemistry have been made over the past five years; however such procedures are still often burdened by substrate specificity and/or incomplete conversions, reducing the fidelity of the resulting libraries. One such reaction is the Heck coupling, for which current DNA-compatible protocols are somewhat unreliable. Utilizing micellar technology, we have developed a highly efficient DNA-compatible Heck reaction that proceeds on average to 95% conversion to product across a broad variety of structurally significant building blocks and multiple DNA conjugates. This work continues the application of micellar catalysis to the development of widely applicable, effective DNA-compatible reactions for use in DELs.
doi_str_mv 10.1021/acs.bioconjchem.3c00051
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subjects Catalysis
Chemical synthesis
Compatibility
Deoxyribonucleic acid
DNA
DNA biosynthesis
Libraries
Substrate specificity
Substrates
title Development of a Micellar-Promoted Heck Reaction for the Synthesis of DNA-Encoded Libraries
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