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Photochemical Transformations of Tetrazole Derivatives: Applications in Organic Synthesis
Tetrazoles remain a challenge to photochemists. Photolysis leads to cleavage of the tetrazolyl ring, may involve various photodegradation pathways and may produce a diversity of photoproducts, depending on the structure and conformational flexibility of the substituents and the possibility of tautom...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257500/ https://www.ncbi.nlm.nih.gov/pubmed/20657512 http://dx.doi.org/10.3390/molecules15053757 |
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author | Frija, Luís Miguel Teodoro Ismael, Amin Cristiano, Maria Lurdes Santos |
author_facet | Frija, Luís Miguel Teodoro Ismael, Amin Cristiano, Maria Lurdes Santos |
author_sort | Frija, Luís Miguel Teodoro |
collection | PubMed |
description | Tetrazoles remain a challenge to photochemists. Photolysis leads to cleavage of the tetrazolyl ring, may involve various photodegradation pathways and may produce a diversity of photoproducts, depending on the structure and conformational flexibility of the substituents and the possibility of tautomerism. If the photochemistry of tetrazoles is considered within the frame of synthetic applications the subject is even more challenging, since the ultimate goal is to achieve selectivity and high yield. In addition, the photoproducts must remain stable and allow isolation or trapping, in order to be used in other reactions. This review summarises the photochemical transformations of tetrazole derivatives that can be used as effective synthetic routes to other compounds. |
format | Online Article Text |
id | pubmed-6257500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62575002019-01-02 Photochemical Transformations of Tetrazole Derivatives: Applications in Organic Synthesis Frija, Luís Miguel Teodoro Ismael, Amin Cristiano, Maria Lurdes Santos Molecules Review Tetrazoles remain a challenge to photochemists. Photolysis leads to cleavage of the tetrazolyl ring, may involve various photodegradation pathways and may produce a diversity of photoproducts, depending on the structure and conformational flexibility of the substituents and the possibility of tautomerism. If the photochemistry of tetrazoles is considered within the frame of synthetic applications the subject is even more challenging, since the ultimate goal is to achieve selectivity and high yield. In addition, the photoproducts must remain stable and allow isolation or trapping, in order to be used in other reactions. This review summarises the photochemical transformations of tetrazole derivatives that can be used as effective synthetic routes to other compounds. MDPI 2010-05-25 /pmc/articles/PMC6257500/ /pubmed/20657512 http://dx.doi.org/10.3390/molecules15053757 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Frija, Luís Miguel Teodoro Ismael, Amin Cristiano, Maria Lurdes Santos Photochemical Transformations of Tetrazole Derivatives: Applications in Organic Synthesis |
title | Photochemical Transformations of Tetrazole Derivatives: Applications in Organic Synthesis |
title_full | Photochemical Transformations of Tetrazole Derivatives: Applications in Organic Synthesis |
title_fullStr | Photochemical Transformations of Tetrazole Derivatives: Applications in Organic Synthesis |
title_full_unstemmed | Photochemical Transformations of Tetrazole Derivatives: Applications in Organic Synthesis |
title_short | Photochemical Transformations of Tetrazole Derivatives: Applications in Organic Synthesis |
title_sort | photochemical transformations of tetrazole derivatives: applications in organic synthesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257500/ https://www.ncbi.nlm.nih.gov/pubmed/20657512 http://dx.doi.org/10.3390/molecules15053757 |
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