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Iridium-Catalyzed Borylation of 6-Fluoroquinolines: Access to 6-Fluoroquinolones
[Image: see text] The Ir-catalyzed C–H borylation of fluoroquinolines has been realized. The quinoline boronic ester formed undergoes a range of important transformations of relevance to medicinal chemistry. Judicious choice of the substituent at C4 on the quinoline facilitated the unmasking of a fl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368603/ https://www.ncbi.nlm.nih.gov/pubmed/35839386 http://dx.doi.org/10.1021/acs.joc.2c00973 |
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author | Hickey, Aobha Merz, Julia Al Mamari, Hamad H. Friedrich, Alexandra Marder, Todd B. McGlacken, Gerard P. |
author_facet | Hickey, Aobha Merz, Julia Al Mamari, Hamad H. Friedrich, Alexandra Marder, Todd B. McGlacken, Gerard P. |
author_sort | Hickey, Aobha |
collection | PubMed |
description | [Image: see text] The Ir-catalyzed C–H borylation of fluoroquinolines has been realized. The quinoline boronic ester formed undergoes a range of important transformations of relevance to medicinal chemistry. Judicious choice of the substituent at C4 on the quinoline facilitated the unmasking of a fluoroquinolone—the core structure of many antibiotics. |
format | Online Article Text |
id | pubmed-9368603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93686032022-08-12 Iridium-Catalyzed Borylation of 6-Fluoroquinolines: Access to 6-Fluoroquinolones Hickey, Aobha Merz, Julia Al Mamari, Hamad H. Friedrich, Alexandra Marder, Todd B. McGlacken, Gerard P. J Org Chem [Image: see text] The Ir-catalyzed C–H borylation of fluoroquinolines has been realized. The quinoline boronic ester formed undergoes a range of important transformations of relevance to medicinal chemistry. Judicious choice of the substituent at C4 on the quinoline facilitated the unmasking of a fluoroquinolone—the core structure of many antibiotics. American Chemical Society 2022-07-15 2022-08-05 /pmc/articles/PMC9368603/ /pubmed/35839386 http://dx.doi.org/10.1021/acs.joc.2c00973 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Hickey, Aobha Merz, Julia Al Mamari, Hamad H. Friedrich, Alexandra Marder, Todd B. McGlacken, Gerard P. Iridium-Catalyzed Borylation of 6-Fluoroquinolines: Access to 6-Fluoroquinolones |
title | Iridium-Catalyzed
Borylation of 6-Fluoroquinolines:
Access to 6-Fluoroquinolones |
title_full | Iridium-Catalyzed
Borylation of 6-Fluoroquinolines:
Access to 6-Fluoroquinolones |
title_fullStr | Iridium-Catalyzed
Borylation of 6-Fluoroquinolines:
Access to 6-Fluoroquinolones |
title_full_unstemmed | Iridium-Catalyzed
Borylation of 6-Fluoroquinolines:
Access to 6-Fluoroquinolones |
title_short | Iridium-Catalyzed
Borylation of 6-Fluoroquinolines:
Access to 6-Fluoroquinolones |
title_sort | iridium-catalyzed
borylation of 6-fluoroquinolines:
access to 6-fluoroquinolones |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368603/ https://www.ncbi.nlm.nih.gov/pubmed/35839386 http://dx.doi.org/10.1021/acs.joc.2c00973 |
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