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Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling
1-[tert-Butyl(diphenyl)silyl]pyrrol-3-ylboronic acid was obtained from pyrrole in three steps. Its Suzuki–Miyaura cross-coupling with functionalized pyridinyl and pyrimidinyl bromides afforded new promising 3-hetaryl-1H-pyrroles.
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241993/ http://dx.doi.org/10.1016/j.mencom.2020.03.034 |
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author | Matyugina, Elena S. Khandazhinskaya, Anastasia L. Kochetkov, Sergey N. Seley-Radtke, Katherine L. |
author_facet | Matyugina, Elena S. Khandazhinskaya, Anastasia L. Kochetkov, Sergey N. Seley-Radtke, Katherine L. |
author_sort | Matyugina, Elena S. |
collection | PubMed |
description | 1-[tert-Butyl(diphenyl)silyl]pyrrol-3-ylboronic acid was obtained from pyrrole in three steps. Its Suzuki–Miyaura cross-coupling with functionalized pyridinyl and pyrimidinyl bromides afforded new promising 3-hetaryl-1H-pyrroles. |
format | Online Article Text |
id | pubmed-7241993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-72419932020-05-22 Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling Matyugina, Elena S. Khandazhinskaya, Anastasia L. Kochetkov, Sergey N. Seley-Radtke, Katherine L. Mendeleev Communications Article 1-[tert-Butyl(diphenyl)silyl]pyrrol-3-ylboronic acid was obtained from pyrrole in three steps. Its Suzuki–Miyaura cross-coupling with functionalized pyridinyl and pyrimidinyl bromides afforded new promising 3-hetaryl-1H-pyrroles. 2020 2020-05-21 /pmc/articles/PMC7241993/ http://dx.doi.org/10.1016/j.mencom.2020.03.034 Text en . Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Matyugina, Elena S. Khandazhinskaya, Anastasia L. Kochetkov, Sergey N. Seley-Radtke, Katherine L. Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling |
title | Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling |
title_full | Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling |
title_fullStr | Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling |
title_full_unstemmed | Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling |
title_short | Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling |
title_sort | synthesis of 3-hetarylpyrroles by suzuki–miyaura cross-coupling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241993/ http://dx.doi.org/10.1016/j.mencom.2020.03.034 |
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