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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-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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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. |
format | Online Article Text |
id | pubmed-10167685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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