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Microwave Assisted Suzuki-Miyaura and Ullmann Type Homocoupling Reactions of 2- and 3-Halopyridines Using a Pd(OAc)(2)/Benzimidazolium Salt and Base Catalyst System
A number of novel benzimidazole derivatives 1–4 were synthesized and the catalytic activity of these compounds in a catalytic system consisting of a benzimidazolium salt/Pd(OAc)(2)/K(2)CO(3) were investigated in the Suzuki-Miyaura and Ullmann type homocoupling reactions under microwave irradiation....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269664/ https://www.ncbi.nlm.nih.gov/pubmed/23529031 http://dx.doi.org/10.3390/molecules18043712 |
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author | Yılmaz, Ülkü Deniz, Selma Küçükbay, Hasan Şireci, Nihat |
author_facet | Yılmaz, Ülkü Deniz, Selma Küçükbay, Hasan Şireci, Nihat |
author_sort | Yılmaz, Ülkü |
collection | PubMed |
description | A number of novel benzimidazole derivatives 1–4 were synthesized and the catalytic activity of these compounds in a catalytic system consisting of a benzimidazolium salt/Pd(OAc)(2)/K(2)CO(3) were investigated in the Suzuki-Miyaura and Ullmann type homocoupling reactions under microwave irradiation. We obtained both cross coupling and homocoupling products of pyridine and some side products such as dimethylaminopyridine and unsubstituted pyridine. |
format | Online Article Text |
id | pubmed-6269664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62696642018-12-14 Microwave Assisted Suzuki-Miyaura and Ullmann Type Homocoupling Reactions of 2- and 3-Halopyridines Using a Pd(OAc)(2)/Benzimidazolium Salt and Base Catalyst System Yılmaz, Ülkü Deniz, Selma Küçükbay, Hasan Şireci, Nihat Molecules Article A number of novel benzimidazole derivatives 1–4 were synthesized and the catalytic activity of these compounds in a catalytic system consisting of a benzimidazolium salt/Pd(OAc)(2)/K(2)CO(3) were investigated in the Suzuki-Miyaura and Ullmann type homocoupling reactions under microwave irradiation. We obtained both cross coupling and homocoupling products of pyridine and some side products such as dimethylaminopyridine and unsubstituted pyridine. MDPI 2013-03-25 /pmc/articles/PMC6269664/ /pubmed/23529031 http://dx.doi.org/10.3390/molecules18043712 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Yılmaz, Ülkü Deniz, Selma Küçükbay, Hasan Şireci, Nihat Microwave Assisted Suzuki-Miyaura and Ullmann Type Homocoupling Reactions of 2- and 3-Halopyridines Using a Pd(OAc)(2)/Benzimidazolium Salt and Base Catalyst System |
title | Microwave Assisted Suzuki-Miyaura and Ullmann Type Homocoupling Reactions of 2- and 3-Halopyridines Using a Pd(OAc)(2)/Benzimidazolium Salt and Base Catalyst System |
title_full | Microwave Assisted Suzuki-Miyaura and Ullmann Type Homocoupling Reactions of 2- and 3-Halopyridines Using a Pd(OAc)(2)/Benzimidazolium Salt and Base Catalyst System |
title_fullStr | Microwave Assisted Suzuki-Miyaura and Ullmann Type Homocoupling Reactions of 2- and 3-Halopyridines Using a Pd(OAc)(2)/Benzimidazolium Salt and Base Catalyst System |
title_full_unstemmed | Microwave Assisted Suzuki-Miyaura and Ullmann Type Homocoupling Reactions of 2- and 3-Halopyridines Using a Pd(OAc)(2)/Benzimidazolium Salt and Base Catalyst System |
title_short | Microwave Assisted Suzuki-Miyaura and Ullmann Type Homocoupling Reactions of 2- and 3-Halopyridines Using a Pd(OAc)(2)/Benzimidazolium Salt and Base Catalyst System |
title_sort | microwave assisted suzuki-miyaura and ullmann type homocoupling reactions of 2- and 3-halopyridines using a pd(oac)(2)/benzimidazolium salt and base catalyst system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269664/ https://www.ncbi.nlm.nih.gov/pubmed/23529031 http://dx.doi.org/10.3390/molecules18043712 |
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