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Suzuki–Miyaura Cross-Coupling of Brominated 2,1-Borazaronaphthalenes with Potassium Alkenyltrifluoroborates
[Image: see text] Conditions have been developed for the palladium-catalyzed cross-coupling of 3-bromo-2,1-borazaronaphthalenes with potassium alkenyltrifluoroborates. Twenty-seven alkenyl-substituted azaborines have been synthesized through this method, providing access to a family of 2,1-borazaron...
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/PMC4242045/ https://www.ncbi.nlm.nih.gov/pubmed/25356980 http://dx.doi.org/10.1021/jo502260x |
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author | Molander, Gary A. Wisniewski, Steven R. Etemadi-Davan, Elham |
author_facet | Molander, Gary A. Wisniewski, Steven R. Etemadi-Davan, Elham |
author_sort | Molander, Gary A. |
collection | PubMed |
description | [Image: see text] Conditions have been developed for the palladium-catalyzed cross-coupling of 3-bromo-2,1-borazaronaphthalenes with potassium alkenyltrifluoroborates. Twenty-seven alkenyl-substituted azaborines have been synthesized through this method, providing access to a family of 2,1-borazaronaphthalenes with alkenyl substitution at the C3 position. |
format | Online Article Text |
id | pubmed-4242045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42420452015-10-30 Suzuki–Miyaura Cross-Coupling of Brominated 2,1-Borazaronaphthalenes with Potassium Alkenyltrifluoroborates Molander, Gary A. Wisniewski, Steven R. Etemadi-Davan, Elham J Org Chem [Image: see text] Conditions have been developed for the palladium-catalyzed cross-coupling of 3-bromo-2,1-borazaronaphthalenes with potassium alkenyltrifluoroborates. Twenty-seven alkenyl-substituted azaborines have been synthesized through this method, providing access to a family of 2,1-borazaronaphthalenes with alkenyl substitution at the C3 position. American Chemical Society 2014-10-30 2014-11-21 /pmc/articles/PMC4242045/ /pubmed/25356980 http://dx.doi.org/10.1021/jo502260x 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 | Molander, Gary A. Wisniewski, Steven R. Etemadi-Davan, Elham Suzuki–Miyaura Cross-Coupling of Brominated 2,1-Borazaronaphthalenes with Potassium Alkenyltrifluoroborates |
title | Suzuki–Miyaura Cross-Coupling of Brominated
2,1-Borazaronaphthalenes with Potassium Alkenyltrifluoroborates |
title_full | Suzuki–Miyaura Cross-Coupling of Brominated
2,1-Borazaronaphthalenes with Potassium Alkenyltrifluoroborates |
title_fullStr | Suzuki–Miyaura Cross-Coupling of Brominated
2,1-Borazaronaphthalenes with Potassium Alkenyltrifluoroborates |
title_full_unstemmed | Suzuki–Miyaura Cross-Coupling of Brominated
2,1-Borazaronaphthalenes with Potassium Alkenyltrifluoroborates |
title_short | Suzuki–Miyaura Cross-Coupling of Brominated
2,1-Borazaronaphthalenes with Potassium Alkenyltrifluoroborates |
title_sort | suzuki–miyaura cross-coupling of brominated
2,1-borazaronaphthalenes with potassium alkenyltrifluoroborates |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4242045/ https://www.ncbi.nlm.nih.gov/pubmed/25356980 http://dx.doi.org/10.1021/jo502260x |
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