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N-Heterocyclic carbene–palladium catalysts for the direct arylation of pyrrole derivatives with aryl chlorides

New Pd–NHC complexes have been synthesized and employed for palladium-catalyzed direct arylation of pyrrole derivatives by using electron-deficient aryl chlorides as coupling partners. The desired coupling products were obtained in moderate to good yields by using 1 mol % of these air-stable palladi...

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Autores principales: Özdemir, Ismail, Gürbüz, Nevin, Kaloğlu, Nazan, Doğan, Öznur, Kaloğlu, Murat, Bruneau, Christian, Doucet, Henri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596014/
https://www.ncbi.nlm.nih.gov/pubmed/23504414
http://dx.doi.org/10.3762/bjoc.9.35
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author Özdemir, Ismail
Gürbüz, Nevin
Kaloğlu, Nazan
Doğan, Öznur
Kaloğlu, Murat
Bruneau, Christian
Doucet, Henri
author_facet Özdemir, Ismail
Gürbüz, Nevin
Kaloğlu, Nazan
Doğan, Öznur
Kaloğlu, Murat
Bruneau, Christian
Doucet, Henri
author_sort Özdemir, Ismail
collection PubMed
description New Pd–NHC complexes have been synthesized and employed for palladium-catalyzed direct arylation of pyrrole derivatives by using electron-deficient aryl chlorides as coupling partners. The desired coupling products were obtained in moderate to good yields by using 1 mol % of these air-stable palladium complexes. This is an advantage compared to the procedures employing air-sensitive phosphines, which have been previously shown to promote the coupling of aryl chlorides with heteroarenes.
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spelling pubmed-35960142013-03-15 N-Heterocyclic carbene–palladium catalysts for the direct arylation of pyrrole derivatives with aryl chlorides Özdemir, Ismail Gürbüz, Nevin Kaloğlu, Nazan Doğan, Öznur Kaloğlu, Murat Bruneau, Christian Doucet, Henri Beilstein J Org Chem Full Research Paper New Pd–NHC complexes have been synthesized and employed for palladium-catalyzed direct arylation of pyrrole derivatives by using electron-deficient aryl chlorides as coupling partners. The desired coupling products were obtained in moderate to good yields by using 1 mol % of these air-stable palladium complexes. This is an advantage compared to the procedures employing air-sensitive phosphines, which have been previously shown to promote the coupling of aryl chlorides with heteroarenes. Beilstein-Institut 2013-02-12 /pmc/articles/PMC3596014/ /pubmed/23504414 http://dx.doi.org/10.3762/bjoc.9.35 Text en Copyright © 2013, Özdemir et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Özdemir, Ismail
Gürbüz, Nevin
Kaloğlu, Nazan
Doğan, Öznur
Kaloğlu, Murat
Bruneau, Christian
Doucet, Henri
N-Heterocyclic carbene–palladium catalysts for the direct arylation of pyrrole derivatives with aryl chlorides
title N-Heterocyclic carbene–palladium catalysts for the direct arylation of pyrrole derivatives with aryl chlorides
title_full N-Heterocyclic carbene–palladium catalysts for the direct arylation of pyrrole derivatives with aryl chlorides
title_fullStr N-Heterocyclic carbene–palladium catalysts for the direct arylation of pyrrole derivatives with aryl chlorides
title_full_unstemmed N-Heterocyclic carbene–palladium catalysts for the direct arylation of pyrrole derivatives with aryl chlorides
title_short N-Heterocyclic carbene–palladium catalysts for the direct arylation of pyrrole derivatives with aryl chlorides
title_sort n-heterocyclic carbene–palladium catalysts for the direct arylation of pyrrole derivatives with aryl chlorides
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596014/
https://www.ncbi.nlm.nih.gov/pubmed/23504414
http://dx.doi.org/10.3762/bjoc.9.35
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