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Tetrazoles via Multicomponent Reactions

[Image: see text] Tetrazole derivatives are a prime class of heterocycles, very important to medicinal chemistry and drug design due to not only their bioisosterism to carboxylic acid and amide moieties but also to their metabolic stability and other beneficial physicochemical properties. Although m...

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Autores principales: Neochoritis, Constantinos G., Zhao, Ting, Dömling, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376451/
https://www.ncbi.nlm.nih.gov/pubmed/30707567
http://dx.doi.org/10.1021/acs.chemrev.8b00564
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author Neochoritis, Constantinos G.
Zhao, Ting
Dömling, Alexander
author_facet Neochoritis, Constantinos G.
Zhao, Ting
Dömling, Alexander
author_sort Neochoritis, Constantinos G.
collection PubMed
description [Image: see text] Tetrazole derivatives are a prime class of heterocycles, very important to medicinal chemistry and drug design due to not only their bioisosterism to carboxylic acid and amide moieties but also to their metabolic stability and other beneficial physicochemical properties. Although more than 20 FDA-approved drugs contain 1H- or 2H-tetrazole substituents, their exact binding mode, structural biology, 3D conformations, and in general their chemical behavior is not fully understood. Importantly, multicomponent reaction (MCR) chemistry offers convergent access to multiple tetrazole scaffolds providing the three important elements of novelty, diversity, and complexity, yet MCR pathways to tetrazoles are far from completely explored. Here, we review the use of multicomponent reactions for the preparation of substituted tetrazole derivatives. We highlight specific applications and general trends holding therein and discuss synthetic approaches and their value by analyzing scope and limitations, and also enlighten their receptor binding mode. Finally, we estimated the prospects of further research in this field.
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spelling pubmed-63764512019-02-19 Tetrazoles via Multicomponent Reactions Neochoritis, Constantinos G. Zhao, Ting Dömling, Alexander Chem Rev [Image: see text] Tetrazole derivatives are a prime class of heterocycles, very important to medicinal chemistry and drug design due to not only their bioisosterism to carboxylic acid and amide moieties but also to their metabolic stability and other beneficial physicochemical properties. Although more than 20 FDA-approved drugs contain 1H- or 2H-tetrazole substituents, their exact binding mode, structural biology, 3D conformations, and in general their chemical behavior is not fully understood. Importantly, multicomponent reaction (MCR) chemistry offers convergent access to multiple tetrazole scaffolds providing the three important elements of novelty, diversity, and complexity, yet MCR pathways to tetrazoles are far from completely explored. Here, we review the use of multicomponent reactions for the preparation of substituted tetrazole derivatives. We highlight specific applications and general trends holding therein and discuss synthetic approaches and their value by analyzing scope and limitations, and also enlighten their receptor binding mode. Finally, we estimated the prospects of further research in this field. American Chemical Society 2019-02-01 2019-02-13 /pmc/articles/PMC6376451/ /pubmed/30707567 http://dx.doi.org/10.1021/acs.chemrev.8b00564 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Neochoritis, Constantinos G.
Zhao, Ting
Dömling, Alexander
Tetrazoles via Multicomponent Reactions
title Tetrazoles via Multicomponent Reactions
title_full Tetrazoles via Multicomponent Reactions
title_fullStr Tetrazoles via Multicomponent Reactions
title_full_unstemmed Tetrazoles via Multicomponent Reactions
title_short Tetrazoles via Multicomponent Reactions
title_sort tetrazoles via multicomponent reactions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376451/
https://www.ncbi.nlm.nih.gov/pubmed/30707567
http://dx.doi.org/10.1021/acs.chemrev.8b00564
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