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Versatile Synthetic Platform for 1,2,3-Triazole Chemistry
[Image: see text] 1,2,3-Triazole scaffolds are not obtained in nature, but they are still intensely investigated by synthetic chemists in various fields due to their excellent properties and green synthetic routes. This review will provide a library of all synthetic routes used in the past 21 years...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608397/ https://www.ncbi.nlm.nih.gov/pubmed/36312377 http://dx.doi.org/10.1021/acsomega.2c04883 |
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author | Vala, Disha P. Vala, Ruturajsinh M. Patel, Hitendra M. |
author_facet | Vala, Disha P. Vala, Ruturajsinh M. Patel, Hitendra M. |
author_sort | Vala, Disha P. |
collection | PubMed |
description | [Image: see text] 1,2,3-Triazole scaffolds are not obtained in nature, but they are still intensely investigated by synthetic chemists in various fields due to their excellent properties and green synthetic routes. This review will provide a library of all synthetic routes used in the past 21 years to synthesize 1,2,3-triazoles and their derivatives using various metal catalysts (such as Cu, Ni, Ru, Ir, Rh, Pd, Au, Ag, Zn, and Sm), organocatalysts, metal-free as well as solvent- and catalyst-free neat syntheses, along with their mechanistic cycles, recyclability studies, solvent systems, and reaction condition effects on regioselectivity. Constant developments indicate that 1,2,3-triazoles will help lead to future organic synthesis and are useful for creating molecular libraries of various functionalized 1,2,3-triazoles. |
format | Online Article Text |
id | pubmed-9608397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96083972022-10-28 Versatile Synthetic Platform for 1,2,3-Triazole Chemistry Vala, Disha P. Vala, Ruturajsinh M. Patel, Hitendra M. ACS Omega [Image: see text] 1,2,3-Triazole scaffolds are not obtained in nature, but they are still intensely investigated by synthetic chemists in various fields due to their excellent properties and green synthetic routes. This review will provide a library of all synthetic routes used in the past 21 years to synthesize 1,2,3-triazoles and their derivatives using various metal catalysts (such as Cu, Ni, Ru, Ir, Rh, Pd, Au, Ag, Zn, and Sm), organocatalysts, metal-free as well as solvent- and catalyst-free neat syntheses, along with their mechanistic cycles, recyclability studies, solvent systems, and reaction condition effects on regioselectivity. Constant developments indicate that 1,2,3-triazoles will help lead to future organic synthesis and are useful for creating molecular libraries of various functionalized 1,2,3-triazoles. American Chemical Society 2022-10-10 /pmc/articles/PMC9608397/ /pubmed/36312377 http://dx.doi.org/10.1021/acsomega.2c04883 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 | Vala, Disha P. Vala, Ruturajsinh M. Patel, Hitendra M. Versatile Synthetic Platform for 1,2,3-Triazole Chemistry |
title | Versatile Synthetic
Platform for 1,2,3-Triazole Chemistry |
title_full | Versatile Synthetic
Platform for 1,2,3-Triazole Chemistry |
title_fullStr | Versatile Synthetic
Platform for 1,2,3-Triazole Chemistry |
title_full_unstemmed | Versatile Synthetic
Platform for 1,2,3-Triazole Chemistry |
title_short | Versatile Synthetic
Platform for 1,2,3-Triazole Chemistry |
title_sort | versatile synthetic
platform for 1,2,3-triazole chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608397/ https://www.ncbi.nlm.nih.gov/pubmed/36312377 http://dx.doi.org/10.1021/acsomega.2c04883 |
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