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MIDA boronate allylation – synthesis of ibuprofen
MIDA boronates are among the most useful reagents for the Suzuki–Miyaura reaction. This chemistry typically generates new bonds between two aromatic rings, thereby restricting access to important areas of chemical space. Here we demonstrate the coupling of MIDA boronates to allylic electrophiles, in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056333/ https://www.ncbi.nlm.nih.gov/pubmed/35516040 http://dx.doi.org/10.1039/d0ra03338c |
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author | Phillips, David Brodie, Glen Memarzadeh, Sarah Tang, Gi Lum France, David J. |
author_facet | Phillips, David Brodie, Glen Memarzadeh, Sarah Tang, Gi Lum France, David J. |
author_sort | Phillips, David |
collection | PubMed |
description | MIDA boronates are among the most useful reagents for the Suzuki–Miyaura reaction. This chemistry typically generates new bonds between two aromatic rings, thereby restricting access to important areas of chemical space. Here we demonstrate the coupling of MIDA boronates to allylic electrophiles, including a new synthesis of the well-known COX inhibitor ibuprofen. |
format | Online Article Text |
id | pubmed-9056333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90563332022-05-04 MIDA boronate allylation – synthesis of ibuprofen Phillips, David Brodie, Glen Memarzadeh, Sarah Tang, Gi Lum France, David J. RSC Adv Chemistry MIDA boronates are among the most useful reagents for the Suzuki–Miyaura reaction. This chemistry typically generates new bonds between two aromatic rings, thereby restricting access to important areas of chemical space. Here we demonstrate the coupling of MIDA boronates to allylic electrophiles, including a new synthesis of the well-known COX inhibitor ibuprofen. The Royal Society of Chemistry 2020-08-18 /pmc/articles/PMC9056333/ /pubmed/35516040 http://dx.doi.org/10.1039/d0ra03338c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Phillips, David Brodie, Glen Memarzadeh, Sarah Tang, Gi Lum France, David J. MIDA boronate allylation – synthesis of ibuprofen |
title | MIDA boronate allylation – synthesis of ibuprofen |
title_full | MIDA boronate allylation – synthesis of ibuprofen |
title_fullStr | MIDA boronate allylation – synthesis of ibuprofen |
title_full_unstemmed | MIDA boronate allylation – synthesis of ibuprofen |
title_short | MIDA boronate allylation – synthesis of ibuprofen |
title_sort | mida boronate allylation – synthesis of ibuprofen |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056333/ https://www.ncbi.nlm.nih.gov/pubmed/35516040 http://dx.doi.org/10.1039/d0ra03338c |
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