Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Swan, Ellen, Platts, Kirsten, Blencowe, Anton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
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
_version_ 1783452938584195072
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
work_keys_str_mv AT swanellen anoverviewofthecycloadditionchemistryoffulvenesandemergingapplications
AT plattskirsten anoverviewofthecycloadditionchemistryoffulvenesandemergingapplications
AT blencoweanton anoverviewofthecycloadditionchemistryoffulvenesandemergingapplications
AT swanellen overviewofthecycloadditionchemistryoffulvenesandemergingapplications
AT plattskirsten overviewofthecycloadditionchemistryoffulvenesandemergingapplications
AT blencoweanton overviewofthecycloadditionchemistryoffulvenesandemergingapplications