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Selected synthetic strategies to cyclophanes

In this review we cover various approaches to meta- and paracyclophanes involving popular reactions. Generally, we have included a strategy where the reaction was used for assembling the cyclophane skeleton for further functionalization. In several instances, after the cyclophane is made several pop...

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Autores principales: Kotha, Sambasivarao, Shirbhate, Mukesh Eknath, Waghule, Gopalkrushna T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578384/
https://www.ncbi.nlm.nih.gov/pubmed/26425186
http://dx.doi.org/10.3762/bjoc.11.142
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author Kotha, Sambasivarao
Shirbhate, Mukesh Eknath
Waghule, Gopalkrushna T
author_facet Kotha, Sambasivarao
Shirbhate, Mukesh Eknath
Waghule, Gopalkrushna T
author_sort Kotha, Sambasivarao
collection PubMed
description In this review we cover various approaches to meta- and paracyclophanes involving popular reactions. Generally, we have included a strategy where the reaction was used for assembling the cyclophane skeleton for further functionalization. In several instances, after the cyclophane is made several popular reactions are used and these are not covered here. We included various natural products related to cyclophanes. To keep the length of the review at a manageable level the literature related to orthocyclophanes was not included.
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spelling pubmed-45783842015-09-30 Selected synthetic strategies to cyclophanes Kotha, Sambasivarao Shirbhate, Mukesh Eknath Waghule, Gopalkrushna T Beilstein J Org Chem Review In this review we cover various approaches to meta- and paracyclophanes involving popular reactions. Generally, we have included a strategy where the reaction was used for assembling the cyclophane skeleton for further functionalization. In several instances, after the cyclophane is made several popular reactions are used and these are not covered here. We included various natural products related to cyclophanes. To keep the length of the review at a manageable level the literature related to orthocyclophanes was not included. Beilstein-Institut 2015-07-29 /pmc/articles/PMC4578384/ /pubmed/26425186 http://dx.doi.org/10.3762/bjoc.11.142 Text en Copyright © 2015, Kotha et al. 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
Kotha, Sambasivarao
Shirbhate, Mukesh Eknath
Waghule, Gopalkrushna T
Selected synthetic strategies to cyclophanes
title Selected synthetic strategies to cyclophanes
title_full Selected synthetic strategies to cyclophanes
title_fullStr Selected synthetic strategies to cyclophanes
title_full_unstemmed Selected synthetic strategies to cyclophanes
title_short Selected synthetic strategies to cyclophanes
title_sort selected synthetic strategies to cyclophanes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578384/
https://www.ncbi.nlm.nih.gov/pubmed/26425186
http://dx.doi.org/10.3762/bjoc.11.142
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