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...
Autores principales: | , , |
---|---|
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 |