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Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement
New β-keto ester substituted stilbene derivatives have been synthesized and cyclized with selenium electrophiles in the presence of Lewis acids. This now allows access to 1,2,3,4-tetrasubstituted naphthalene derivatives as cyclization and rearrangement products.
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272767/ https://www.ncbi.nlm.nih.gov/pubmed/26076108 http://dx.doi.org/10.3390/molecules200610866 |
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author | Tancock, James Wirth, Thomas |
author_facet | Tancock, James Wirth, Thomas |
author_sort | Tancock, James |
collection | PubMed |
description | New β-keto ester substituted stilbene derivatives have been synthesized and cyclized with selenium electrophiles in the presence of Lewis acids. This now allows access to 1,2,3,4-tetrasubstituted naphthalene derivatives as cyclization and rearrangement products. |
format | Online Article Text |
id | pubmed-6272767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62727672018-12-31 Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement Tancock, James Wirth, Thomas Molecules Communication New β-keto ester substituted stilbene derivatives have been synthesized and cyclized with selenium electrophiles in the presence of Lewis acids. This now allows access to 1,2,3,4-tetrasubstituted naphthalene derivatives as cyclization and rearrangement products. MDPI 2015-06-12 /pmc/articles/PMC6272767/ /pubmed/26076108 http://dx.doi.org/10.3390/molecules200610866 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Tancock, James Wirth, Thomas Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement |
title | Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement |
title_full | Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement |
title_fullStr | Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement |
title_full_unstemmed | Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement |
title_short | Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement |
title_sort | selenium-mediated synthesis of tetrasubstituted naphthalenes through rearrangement |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272767/ https://www.ncbi.nlm.nih.gov/pubmed/26076108 http://dx.doi.org/10.3390/molecules200610866 |
work_keys_str_mv | AT tancockjames seleniummediatedsynthesisoftetrasubstitutednaphthalenesthroughrearrangement AT wirththomas seleniummediatedsynthesisoftetrasubstitutednaphthalenesthroughrearrangement |