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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...

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Autores principales: Vala, Disha P., Vala, Ruturajsinh M., Patel, Hitendra M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
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.
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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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