Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1783395560890302464 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6376451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT neochoritisconstantinosg tetrazolesviamulticomponentreactions AT zhaoting tetrazolesviamulticomponentreactions AT domlingalexander tetrazolesviamulticomponentreactions |