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Coumarin–Tetrapyrrolic Macrocycle Conjugates: Synthesis and Applications

This review covers the synthesis of coumarin–porphyrin, coumarin–phthalocyanine and coumarin–corrole conjugates and their potential applications. While coumarin–phthalocyanine conjugates were obtained almost exclusively by tetramerization of coumarin-functionalized phthalonitriles, coumarin–porphyri...

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Autores principales: Cerqueira, Ana F. R., Almodôvar, Vítor A. S., Neves, Maria G. P. M. S., Tomé, Augusto C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152750/
https://www.ncbi.nlm.nih.gov/pubmed/28617340
http://dx.doi.org/10.3390/molecules22060994
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author Cerqueira, Ana F. R.
Almodôvar, Vítor A. S.
Neves, Maria G. P. M. S.
Tomé, Augusto C.
author_facet Cerqueira, Ana F. R.
Almodôvar, Vítor A. S.
Neves, Maria G. P. M. S.
Tomé, Augusto C.
author_sort Cerqueira, Ana F. R.
collection PubMed
description This review covers the synthesis of coumarin–porphyrin, coumarin–phthalocyanine and coumarin–corrole conjugates and their potential applications. While coumarin–phthalocyanine conjugates were obtained almost exclusively by tetramerization of coumarin-functionalized phthalonitriles, coumarin–porphyrin and coumarin–corrole conjugates were prepared by complementary approaches: (a) direct synthesis of the tetrapyrrolic macrocycle using formylcoumarins and pyrrole or (b) by functionalization of the tetrapyrrolic macrocycle. In the last approach a range of reaction types were used, namely 1,3-dipolar cycloadditions, hetero-Diels–Alder, Sonogashira, alkylation or acylation reactions. This is clearly a more versatile approach, leading to a larger diversity of conjugates and allowing the access to conjugates bearing one to up to 16 coumarin units.
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spelling pubmed-61527502018-11-13 Coumarin–Tetrapyrrolic Macrocycle Conjugates: Synthesis and Applications Cerqueira, Ana F. R. Almodôvar, Vítor A. S. Neves, Maria G. P. M. S. Tomé, Augusto C. Molecules Review This review covers the synthesis of coumarin–porphyrin, coumarin–phthalocyanine and coumarin–corrole conjugates and their potential applications. While coumarin–phthalocyanine conjugates were obtained almost exclusively by tetramerization of coumarin-functionalized phthalonitriles, coumarin–porphyrin and coumarin–corrole conjugates were prepared by complementary approaches: (a) direct synthesis of the tetrapyrrolic macrocycle using formylcoumarins and pyrrole or (b) by functionalization of the tetrapyrrolic macrocycle. In the last approach a range of reaction types were used, namely 1,3-dipolar cycloadditions, hetero-Diels–Alder, Sonogashira, alkylation or acylation reactions. This is clearly a more versatile approach, leading to a larger diversity of conjugates and allowing the access to conjugates bearing one to up to 16 coumarin units. MDPI 2017-06-15 /pmc/articles/PMC6152750/ /pubmed/28617340 http://dx.doi.org/10.3390/molecules22060994 Text en © 2017 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Cerqueira, Ana F. R.
Almodôvar, Vítor A. S.
Neves, Maria G. P. M. S.
Tomé, Augusto C.
Coumarin–Tetrapyrrolic Macrocycle Conjugates: Synthesis and Applications
title Coumarin–Tetrapyrrolic Macrocycle Conjugates: Synthesis and Applications
title_full Coumarin–Tetrapyrrolic Macrocycle Conjugates: Synthesis and Applications
title_fullStr Coumarin–Tetrapyrrolic Macrocycle Conjugates: Synthesis and Applications
title_full_unstemmed Coumarin–Tetrapyrrolic Macrocycle Conjugates: Synthesis and Applications
title_short Coumarin–Tetrapyrrolic Macrocycle Conjugates: Synthesis and Applications
title_sort coumarin–tetrapyrrolic macrocycle conjugates: synthesis and applications
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152750/
https://www.ncbi.nlm.nih.gov/pubmed/28617340
http://dx.doi.org/10.3390/molecules22060994
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