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Aminooxy Click Chemistry as a Tool for Bis-homo and Bis-hetero Ligand Conjugation to Nucleic Acids

[Image: see text] An aminooxy click chemistry (AOCC) strategy was used to synthesize nucleoside building blocks for incorporation during solid-support synthesis of oligonucleotides to enable bis-homo and bis-hetero conjugation of various biologically relevant ligands. The bis-homo aminooxy conjugati...

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Autores principales: Datta, Dhrubajyoti, Mori, Shohei, Madaoui, Mimouna, Wassarman, Kelly, Zlatev, Ivan, Manoharan, Muthiah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251770/
https://www.ncbi.nlm.nih.gov/pubmed/35715221
http://dx.doi.org/10.1021/acs.orglett.2c00988
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author Datta, Dhrubajyoti
Mori, Shohei
Madaoui, Mimouna
Wassarman, Kelly
Zlatev, Ivan
Manoharan, Muthiah
author_facet Datta, Dhrubajyoti
Mori, Shohei
Madaoui, Mimouna
Wassarman, Kelly
Zlatev, Ivan
Manoharan, Muthiah
author_sort Datta, Dhrubajyoti
collection PubMed
description [Image: see text] An aminooxy click chemistry (AOCC) strategy was used to synthesize nucleoside building blocks for incorporation during solid-support synthesis of oligonucleotides to enable bis-homo and bis-hetero conjugation of various biologically relevant ligands. The bis-homo aminooxy conjugation leads to bivalent ligand presentation, whereas the bis-hetero conjugation allows the placement of different ligands with either the same or different chemical linkages. This facile synthetic methodology allows introduction of two different ligands with different biological functions simultaneously.
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spelling pubmed-92517702022-07-05 Aminooxy Click Chemistry as a Tool for Bis-homo and Bis-hetero Ligand Conjugation to Nucleic Acids Datta, Dhrubajyoti Mori, Shohei Madaoui, Mimouna Wassarman, Kelly Zlatev, Ivan Manoharan, Muthiah Org Lett [Image: see text] An aminooxy click chemistry (AOCC) strategy was used to synthesize nucleoside building blocks for incorporation during solid-support synthesis of oligonucleotides to enable bis-homo and bis-hetero conjugation of various biologically relevant ligands. The bis-homo aminooxy conjugation leads to bivalent ligand presentation, whereas the bis-hetero conjugation allows the placement of different ligands with either the same or different chemical linkages. This facile synthetic methodology allows introduction of two different ligands with different biological functions simultaneously. American Chemical Society 2022-06-17 2022-07-01 /pmc/articles/PMC9251770/ /pubmed/35715221 http://dx.doi.org/10.1021/acs.orglett.2c00988 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Datta, Dhrubajyoti
Mori, Shohei
Madaoui, Mimouna
Wassarman, Kelly
Zlatev, Ivan
Manoharan, Muthiah
Aminooxy Click Chemistry as a Tool for Bis-homo and Bis-hetero Ligand Conjugation to Nucleic Acids
title Aminooxy Click Chemistry as a Tool for Bis-homo and Bis-hetero Ligand Conjugation to Nucleic Acids
title_full Aminooxy Click Chemistry as a Tool for Bis-homo and Bis-hetero Ligand Conjugation to Nucleic Acids
title_fullStr Aminooxy Click Chemistry as a Tool for Bis-homo and Bis-hetero Ligand Conjugation to Nucleic Acids
title_full_unstemmed Aminooxy Click Chemistry as a Tool for Bis-homo and Bis-hetero Ligand Conjugation to Nucleic Acids
title_short Aminooxy Click Chemistry as a Tool for Bis-homo and Bis-hetero Ligand Conjugation to Nucleic Acids
title_sort aminooxy click chemistry as a tool for bis-homo and bis-hetero ligand conjugation to nucleic acids
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251770/
https://www.ncbi.nlm.nih.gov/pubmed/35715221
http://dx.doi.org/10.1021/acs.orglett.2c00988
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