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Syntheses of Cyclotriveratrylene Analogues and Their Long Elusive Triketone Congeners
[Image: see text] Although interest in cyclotriveratrylene and its analogues has been significant, limitations in the ability to adjust its structure fully have hampered studies into their complete range of properties. A unique strategy to synthesize a previously unobtainable cyclotriveratrylene ana...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4334237/ https://www.ncbi.nlm.nih.gov/pubmed/24987807 http://dx.doi.org/10.1021/ol501284s |
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author | Wright, Nathan E. ElSohly, Adel M. Snyder, Scott A. |
author_facet | Wright, Nathan E. ElSohly, Adel M. Snyder, Scott A. |
author_sort | Wright, Nathan E. |
collection | PubMed |
description | [Image: see text] Although interest in cyclotriveratrylene and its analogues has been significant, limitations in the ability to adjust its structure fully have hampered studies into their complete range of properties. A unique strategy to synthesize a previously unobtainable cyclotriveratrylene analogue and a procedure which adjusts the inner methylene bridges of that material to a triketone is reported. A second triketone synthesis and computational studies indicate the parameters needed for success. |
format | Online Article Text |
id | pubmed-4334237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-43342372015-07-02 Syntheses of Cyclotriveratrylene Analogues and Their Long Elusive Triketone Congeners Wright, Nathan E. ElSohly, Adel M. Snyder, Scott A. Org Lett [Image: see text] Although interest in cyclotriveratrylene and its analogues has been significant, limitations in the ability to adjust its structure fully have hampered studies into their complete range of properties. A unique strategy to synthesize a previously unobtainable cyclotriveratrylene analogue and a procedure which adjusts the inner methylene bridges of that material to a triketone is reported. A second triketone synthesis and computational studies indicate the parameters needed for success. American Chemical Society 2014-07-02 2014-07-18 /pmc/articles/PMC4334237/ /pubmed/24987807 http://dx.doi.org/10.1021/ol501284s Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Wright, Nathan E. ElSohly, Adel M. Snyder, Scott A. Syntheses of Cyclotriveratrylene Analogues and Their Long Elusive Triketone Congeners |
title | Syntheses of Cyclotriveratrylene Analogues and Their
Long Elusive Triketone Congeners |
title_full | Syntheses of Cyclotriveratrylene Analogues and Their
Long Elusive Triketone Congeners |
title_fullStr | Syntheses of Cyclotriveratrylene Analogues and Their
Long Elusive Triketone Congeners |
title_full_unstemmed | Syntheses of Cyclotriveratrylene Analogues and Their
Long Elusive Triketone Congeners |
title_short | Syntheses of Cyclotriveratrylene Analogues and Their
Long Elusive Triketone Congeners |
title_sort | syntheses of cyclotriveratrylene analogues and their
long elusive triketone congeners |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4334237/ https://www.ncbi.nlm.nih.gov/pubmed/24987807 http://dx.doi.org/10.1021/ol501284s |
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