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An overview of the cycloaddition chemistry of fulvenes and emerging applications
The unusual electronic properties and unique reactivity of fulvenes have interested researchers for over a century. The propensity to form dipolar structures at relatively low temperatures and to participate as various components in cycloaddition reactions, often highly selectively, makes them ideal...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753682/ https://www.ncbi.nlm.nih.gov/pubmed/31579091 http://dx.doi.org/10.3762/bjoc.15.209 |
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author | Swan, Ellen Platts, Kirsten Blencowe, Anton |
author_facet | Swan, Ellen Platts, Kirsten Blencowe, Anton |
author_sort | Swan, Ellen |
collection | PubMed |
description | The unusual electronic properties and unique reactivity of fulvenes have interested researchers for over a century. The propensity to form dipolar structures at relatively low temperatures and to participate as various components in cycloaddition reactions, often highly selectively, makes them ideal for the synthesis of complex polycyclic carbon scaffolds. As a result, fulvene cycloaddition chemistry has been employed extensively for the synthesis of natural products. More recently, fulvene cycloaddition chemistry has also found application to other areas including materials chemistry and dynamic combinatorial chemistry. This highlight article discusses the unusual properties of fulvenes and their varied cycloaddition chemistry, focussing on applications in organic and natural synthesis, dynamic combinatorial chemistry and materials chemistry, including dynamers, hydrogels and charge transfer complexes. Tables providing comprehensive directories of fulvene cycloaddition chemistry are provided, including fulvene intramolecular and intermolecular cycloadditions complete with reactant partners and their resulting cyclic adducts, which provide a useful reference source for synthetic chemists working with fulvenes and complex polycyclic scaffolds. |
format | Online Article Text |
id | pubmed-6753682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-67536822019-10-02 An overview of the cycloaddition chemistry of fulvenes and emerging applications Swan, Ellen Platts, Kirsten Blencowe, Anton Beilstein J Org Chem Review The unusual electronic properties and unique reactivity of fulvenes have interested researchers for over a century. The propensity to form dipolar structures at relatively low temperatures and to participate as various components in cycloaddition reactions, often highly selectively, makes them ideal for the synthesis of complex polycyclic carbon scaffolds. As a result, fulvene cycloaddition chemistry has been employed extensively for the synthesis of natural products. More recently, fulvene cycloaddition chemistry has also found application to other areas including materials chemistry and dynamic combinatorial chemistry. This highlight article discusses the unusual properties of fulvenes and their varied cycloaddition chemistry, focussing on applications in organic and natural synthesis, dynamic combinatorial chemistry and materials chemistry, including dynamers, hydrogels and charge transfer complexes. Tables providing comprehensive directories of fulvene cycloaddition chemistry are provided, including fulvene intramolecular and intermolecular cycloadditions complete with reactant partners and their resulting cyclic adducts, which provide a useful reference source for synthetic chemists working with fulvenes and complex polycyclic scaffolds. Beilstein-Institut 2019-09-06 /pmc/articles/PMC6753682/ /pubmed/31579091 http://dx.doi.org/10.3762/bjoc.15.209 Text en Copyright © 2019, Swan et al. https://creativecommons.org/licenses/by/4.0https://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/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Review Swan, Ellen Platts, Kirsten Blencowe, Anton An overview of the cycloaddition chemistry of fulvenes and emerging applications |
title | An overview of the cycloaddition chemistry of fulvenes and emerging applications |
title_full | An overview of the cycloaddition chemistry of fulvenes and emerging applications |
title_fullStr | An overview of the cycloaddition chemistry of fulvenes and emerging applications |
title_full_unstemmed | An overview of the cycloaddition chemistry of fulvenes and emerging applications |
title_short | An overview of the cycloaddition chemistry of fulvenes and emerging applications |
title_sort | overview of the cycloaddition chemistry of fulvenes and emerging applications |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753682/ https://www.ncbi.nlm.nih.gov/pubmed/31579091 http://dx.doi.org/10.3762/bjoc.15.209 |
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