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Solid-Phase Synthesis of s-Tetrazines

[Image: see text] An efficient synthesis of s-tetrazines by solid-phase methods is described. This synthesis route was compatible with different solid-phase resins and linkers and did not require metal catalysts or high temperatures. Monosubstituted tetrazines were routinely synthesized using thiol-...

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Autores principales: Alghamdi, Zainab S., Klausen, Maxime, Gambardella, Alessia, Lilienkampf, Annamaria, Bradley, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10167685/
https://www.ncbi.nlm.nih.gov/pubmed/37083299
http://dx.doi.org/10.1021/acs.orglett.3c00955
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author Alghamdi, Zainab S.
Klausen, Maxime
Gambardella, Alessia
Lilienkampf, Annamaria
Bradley, Mark
author_facet Alghamdi, Zainab S.
Klausen, Maxime
Gambardella, Alessia
Lilienkampf, Annamaria
Bradley, Mark
author_sort Alghamdi, Zainab S.
collection PubMed
description [Image: see text] An efficient synthesis of s-tetrazines by solid-phase methods is described. This synthesis route was compatible with different solid-phase resins and linkers and did not require metal catalysts or high temperatures. Monosubstituted tetrazines were routinely synthesized using thiol-promoted chemistry, using dichloromethane as a carbon source, while disubstituted unsymmetrical aryl or alkyl tetrazines were synthesized using readily available nitriles. This efficient approach enabled the synthesis of s-tetrazines in high yields (70–94%), eliminating the classical solution-phase problems of mixtures of symmetrical and unsymmetrical tetrazines, with only a single final purification step required, and paves the way to the rapid synthesis of s-tetrazines with various applications in bioorthogonal chemistry and beyond.
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spelling pubmed-101676852023-05-10 Solid-Phase Synthesis of s-Tetrazines Alghamdi, Zainab S. Klausen, Maxime Gambardella, Alessia Lilienkampf, Annamaria Bradley, Mark Org Lett [Image: see text] An efficient synthesis of s-tetrazines by solid-phase methods is described. This synthesis route was compatible with different solid-phase resins and linkers and did not require metal catalysts or high temperatures. Monosubstituted tetrazines were routinely synthesized using thiol-promoted chemistry, using dichloromethane as a carbon source, while disubstituted unsymmetrical aryl or alkyl tetrazines were synthesized using readily available nitriles. This efficient approach enabled the synthesis of s-tetrazines in high yields (70–94%), eliminating the classical solution-phase problems of mixtures of symmetrical and unsymmetrical tetrazines, with only a single final purification step required, and paves the way to the rapid synthesis of s-tetrazines with various applications in bioorthogonal chemistry and beyond. American Chemical Society 2023-04-21 /pmc/articles/PMC10167685/ /pubmed/37083299 http://dx.doi.org/10.1021/acs.orglett.3c00955 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Alghamdi, Zainab S.
Klausen, Maxime
Gambardella, Alessia
Lilienkampf, Annamaria
Bradley, Mark
Solid-Phase Synthesis of s-Tetrazines
title Solid-Phase Synthesis of s-Tetrazines
title_full Solid-Phase Synthesis of s-Tetrazines
title_fullStr Solid-Phase Synthesis of s-Tetrazines
title_full_unstemmed Solid-Phase Synthesis of s-Tetrazines
title_short Solid-Phase Synthesis of s-Tetrazines
title_sort solid-phase synthesis of s-tetrazines
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10167685/
https://www.ncbi.nlm.nih.gov/pubmed/37083299
http://dx.doi.org/10.1021/acs.orglett.3c00955
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