Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities

Correction for ‘Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytot...

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Detalles Bibliográficos
Autores principales: Touj, Nedra, Al-Ayed, Abdullah S., Sauthier, Mathieu, Mansour, Lamjed, Harrath, Abdel Halim, Al-Tamimi, Jameel, Özdemir, Ismail, Yaşar, Sedat, Hamdi, Naceur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059531/
https://www.ncbi.nlm.nih.gov/pubmed/35532490
http://dx.doi.org/10.1039/c8ra90103a
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author Touj, Nedra
Al-Ayed, Abdullah S.
Sauthier, Mathieu
Mansour, Lamjed
Harrath, Abdel Halim
Al-Tamimi, Jameel
Özdemir, Ismail
Yaşar, Sedat
Hamdi, Naceur
author_facet Touj, Nedra
Al-Ayed, Abdullah S.
Sauthier, Mathieu
Mansour, Lamjed
Harrath, Abdel Halim
Al-Tamimi, Jameel
Özdemir, Ismail
Yaşar, Sedat
Hamdi, Naceur
author_sort Touj, Nedra
collection PubMed
description Correction for ‘Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities’ by Nedra Touj et al., RSC Adv., 2018, 8, 40000–40015.
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spelling pubmed-90595312022-05-04 Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities Touj, Nedra Al-Ayed, Abdullah S. Sauthier, Mathieu Mansour, Lamjed Harrath, Abdel Halim Al-Tamimi, Jameel Özdemir, Ismail Yaşar, Sedat Hamdi, Naceur RSC Adv Chemistry Correction for ‘Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities’ by Nedra Touj et al., RSC Adv., 2018, 8, 40000–40015. The Royal Society of Chemistry 2018-12-21 /pmc/articles/PMC9059531/ /pubmed/35532490 http://dx.doi.org/10.1039/c8ra90103a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Touj, Nedra
Al-Ayed, Abdullah S.
Sauthier, Mathieu
Mansour, Lamjed
Harrath, Abdel Halim
Al-Tamimi, Jameel
Özdemir, Ismail
Yaşar, Sedat
Hamdi, Naceur
Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities
title Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities
title_full Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities
title_fullStr Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities
title_full_unstemmed Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities
title_short Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities
title_sort correction: efficient in situ n-heterocyclic carbene palladium(ii) generated from pd(oac)(2) catalysts for carbonylative suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059531/
https://www.ncbi.nlm.nih.gov/pubmed/35532490
http://dx.doi.org/10.1039/c8ra90103a
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