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Suzuki Cross-Coupling of [2.2]Paracyclophane Trifluoroborates with Pyridyl and Pyrimidyl Building Blocks
[Image: see text] We report a new Suzuki cross-coupling protocol for high yielding derivatization of [2.2]paracyclophane with pyridyl and pyrimidyl substituents. The [2.2]paracyclophane trifluoroborate salt presented herein is a bench stable, easily accessible, and convenient substitute to former cr...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645350/ https://www.ncbi.nlm.nih.gov/pubmed/31459290 http://dx.doi.org/10.1021/acsomega.8b01774 |
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author | Knoll, Daniel M. Bräse, Stefan |
author_facet | Knoll, Daniel M. Bräse, Stefan |
author_sort | Knoll, Daniel M. |
collection | PubMed |
description | [Image: see text] We report a new Suzuki cross-coupling protocol for high yielding derivatization of [2.2]paracyclophane with pyridyl and pyrimidyl substituents. The [2.2]paracyclophane trifluoroborate salt presented herein is a bench stable, easily accessible, and convenient substitute to former cross-coupling substrates. This will be of very high interest for future paracyclophane derivatization endeavors. |
format | Online Article Text |
id | pubmed-6645350 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66453502019-08-27 Suzuki Cross-Coupling of [2.2]Paracyclophane Trifluoroborates with Pyridyl and Pyrimidyl Building Blocks Knoll, Daniel M. Bräse, Stefan ACS Omega [Image: see text] We report a new Suzuki cross-coupling protocol for high yielding derivatization of [2.2]paracyclophane with pyridyl and pyrimidyl substituents. The [2.2]paracyclophane trifluoroborate salt presented herein is a bench stable, easily accessible, and convenient substitute to former cross-coupling substrates. This will be of very high interest for future paracyclophane derivatization endeavors. American Chemical Society 2018-09-27 /pmc/articles/PMC6645350/ /pubmed/31459290 http://dx.doi.org/10.1021/acsomega.8b01774 Text en Copyright © 2018 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 | Knoll, Daniel M. Bräse, Stefan Suzuki Cross-Coupling of [2.2]Paracyclophane Trifluoroborates with Pyridyl and Pyrimidyl Building Blocks |
title | Suzuki Cross-Coupling of [2.2]Paracyclophane Trifluoroborates
with Pyridyl and Pyrimidyl Building Blocks |
title_full | Suzuki Cross-Coupling of [2.2]Paracyclophane Trifluoroborates
with Pyridyl and Pyrimidyl Building Blocks |
title_fullStr | Suzuki Cross-Coupling of [2.2]Paracyclophane Trifluoroborates
with Pyridyl and Pyrimidyl Building Blocks |
title_full_unstemmed | Suzuki Cross-Coupling of [2.2]Paracyclophane Trifluoroborates
with Pyridyl and Pyrimidyl Building Blocks |
title_short | Suzuki Cross-Coupling of [2.2]Paracyclophane Trifluoroborates
with Pyridyl and Pyrimidyl Building Blocks |
title_sort | suzuki cross-coupling of [2.2]paracyclophane trifluoroborates
with pyridyl and pyrimidyl building blocks |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645350/ https://www.ncbi.nlm.nih.gov/pubmed/31459290 http://dx.doi.org/10.1021/acsomega.8b01774 |
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