Cargando…

Copper(I)-Catalyzed Alkyne–Azide Cycloaddition (CuAAC) “Click” Reaction: A Powerful Tool for Functionalizing Polyhydroxylated Platforms

[Image: see text] Click chemistry is currently one of the most used tools for the generation of complex organic molecules. The advantages of using click chemistry in organic synthesis are remarkable; in many cases, the reactions occur under mild conditions and are free of solvents, with high yields...

Descripción completa

Detalles Bibliográficos
Autores principales: Pineda-Castañeda, Héctor Manuel, Rivera-Monroy, Zuly Jenny, Maldonado, Mauricio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9893463/
https://www.ncbi.nlm.nih.gov/pubmed/36743057
http://dx.doi.org/10.1021/acsomega.2c06269
_version_ 1784881532554444800
author Pineda-Castañeda, Héctor Manuel
Rivera-Monroy, Zuly Jenny
Maldonado, Mauricio
author_facet Pineda-Castañeda, Héctor Manuel
Rivera-Monroy, Zuly Jenny
Maldonado, Mauricio
author_sort Pineda-Castañeda, Héctor Manuel
collection PubMed
description [Image: see text] Click chemistry is currently one of the most used tools for the generation of complex organic molecules. The advantages of using click chemistry in organic synthesis are remarkable; in many cases, the reactions occur under mild conditions and are free of solvents, with high yields and short reaction times. This makes it an extraordinarily effective and viable alternative for obtaining complex/conjugated molecules. In this review, the use of click chemistry CuAAC is especially emphasized for polyhydroxylated platforms such as resorcinarenes or calixarenes, focusing mainly on aspects of synthesis, specifically conditions, reagents, and methodologies.
format Online
Article
Text
id pubmed-9893463
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-98934632023-02-03 Copper(I)-Catalyzed Alkyne–Azide Cycloaddition (CuAAC) “Click” Reaction: A Powerful Tool for Functionalizing Polyhydroxylated Platforms Pineda-Castañeda, Héctor Manuel Rivera-Monroy, Zuly Jenny Maldonado, Mauricio ACS Omega [Image: see text] Click chemistry is currently one of the most used tools for the generation of complex organic molecules. The advantages of using click chemistry in organic synthesis are remarkable; in many cases, the reactions occur under mild conditions and are free of solvents, with high yields and short reaction times. This makes it an extraordinarily effective and viable alternative for obtaining complex/conjugated molecules. In this review, the use of click chemistry CuAAC is especially emphasized for polyhydroxylated platforms such as resorcinarenes or calixarenes, focusing mainly on aspects of synthesis, specifically conditions, reagents, and methodologies. American Chemical Society 2023-01-18 /pmc/articles/PMC9893463/ /pubmed/36743057 http://dx.doi.org/10.1021/acsomega.2c06269 Text en © 2023 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 Pineda-Castañeda, Héctor Manuel
Rivera-Monroy, Zuly Jenny
Maldonado, Mauricio
Copper(I)-Catalyzed Alkyne–Azide Cycloaddition (CuAAC) “Click” Reaction: A Powerful Tool for Functionalizing Polyhydroxylated Platforms
title Copper(I)-Catalyzed Alkyne–Azide Cycloaddition (CuAAC) “Click” Reaction: A Powerful Tool for Functionalizing Polyhydroxylated Platforms
title_full Copper(I)-Catalyzed Alkyne–Azide Cycloaddition (CuAAC) “Click” Reaction: A Powerful Tool for Functionalizing Polyhydroxylated Platforms
title_fullStr Copper(I)-Catalyzed Alkyne–Azide Cycloaddition (CuAAC) “Click” Reaction: A Powerful Tool for Functionalizing Polyhydroxylated Platforms
title_full_unstemmed Copper(I)-Catalyzed Alkyne–Azide Cycloaddition (CuAAC) “Click” Reaction: A Powerful Tool for Functionalizing Polyhydroxylated Platforms
title_short Copper(I)-Catalyzed Alkyne–Azide Cycloaddition (CuAAC) “Click” Reaction: A Powerful Tool for Functionalizing Polyhydroxylated Platforms
title_sort copper(i)-catalyzed alkyne–azide cycloaddition (cuaac) “click” reaction: a powerful tool for functionalizing polyhydroxylated platforms
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9893463/
https://www.ncbi.nlm.nih.gov/pubmed/36743057
http://dx.doi.org/10.1021/acsomega.2c06269
work_keys_str_mv AT pinedacastanedahectormanuel coppericatalyzedalkyneazidecycloadditioncuaacclickreactionapowerfultoolforfunctionalizingpolyhydroxylatedplatforms
AT riveramonroyzulyjenny coppericatalyzedalkyneazidecycloadditioncuaacclickreactionapowerfultoolforfunctionalizingpolyhydroxylatedplatforms
AT maldonadomauricio coppericatalyzedalkyneazidecycloadditioncuaacclickreactionapowerfultoolforfunctionalizingpolyhydroxylatedplatforms