Syntheses and applications of furanyl-functionalised 2,2’:6’,2’’-terpyridines

Different synthetic routes leading to terpyridines functionalised with furan heterocycles are reviewed. The methodologies used to prepare such compounds include the ring closure of 1,5-diketones and cross-coupling reactions. These versatile terpyridines and their derived metal complexes find applica...

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Detalles Bibliográficos
Autores principales: Husson, Jérôme, Knorr, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326614/
https://www.ncbi.nlm.nih.gov/pubmed/22509206
http://dx.doi.org/10.3762/bjoc.8.41
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author Husson, Jérôme
Knorr, Michael
author_facet Husson, Jérôme
Knorr, Michael
author_sort Husson, Jérôme
collection PubMed
description Different synthetic routes leading to terpyridines functionalised with furan heterocycles are reviewed. The methodologies used to prepare such compounds include the ring closure of 1,5-diketones and cross-coupling reactions. These versatile terpyridines and their derived metal complexes find applications in various fields including coordination chemistry, medicinal chemistry and material sciences.
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spelling pubmed-33266142012-04-16 Syntheses and applications of furanyl-functionalised 2,2’:6’,2’’-terpyridines Husson, Jérôme Knorr, Michael Beilstein J Org Chem Review Different synthetic routes leading to terpyridines functionalised with furan heterocycles are reviewed. The methodologies used to prepare such compounds include the ring closure of 1,5-diketones and cross-coupling reactions. These versatile terpyridines and their derived metal complexes find applications in various fields including coordination chemistry, medicinal chemistry and material sciences. Beilstein-Institut 2012-03-12 /pmc/articles/PMC3326614/ /pubmed/22509206 http://dx.doi.org/10.3762/bjoc.8.41 Text en Copyright © 2012, Husson and Knorr https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Husson, Jérôme
Knorr, Michael
Syntheses and applications of furanyl-functionalised 2,2’:6’,2’’-terpyridines
title Syntheses and applications of furanyl-functionalised 2,2’:6’,2’’-terpyridines
title_full Syntheses and applications of furanyl-functionalised 2,2’:6’,2’’-terpyridines
title_fullStr Syntheses and applications of furanyl-functionalised 2,2’:6’,2’’-terpyridines
title_full_unstemmed Syntheses and applications of furanyl-functionalised 2,2’:6’,2’’-terpyridines
title_short Syntheses and applications of furanyl-functionalised 2,2’:6’,2’’-terpyridines
title_sort syntheses and applications of furanyl-functionalised 2,2’:6’,2’’-terpyridines
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326614/
https://www.ncbi.nlm.nih.gov/pubmed/22509206
http://dx.doi.org/10.3762/bjoc.8.41
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