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Palladium-catalyzed α-arylation of carbonyls in the de novo synthesis of aromatic heterocycles
Aromatic heterocycles are a very well represented motif in natural products and have found various applications in chemistry and material science, as well as being commonly found in pharmaceutical agents. Thus, new and efficient routes towards this class of compound are always desirable, particularl...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424829/ https://www.ncbi.nlm.nih.gov/pubmed/25789887 http://dx.doi.org/10.1039/c5ob00055f |
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author | Potukuchi, Harish K. Spork, Anatol P. Donohoe, Timothy J. |
author_facet | Potukuchi, Harish K. Spork, Anatol P. Donohoe, Timothy J. |
author_sort | Potukuchi, Harish K. |
collection | PubMed |
description | Aromatic heterocycles are a very well represented motif in natural products and have found various applications in chemistry and material science, as well as being commonly found in pharmaceutical agents. Thus, new and efficient routes towards this class of compound are always desirable, particularly if they expand the scope of chemical methodology or facilitate more effective pathways to complex substitution patterns. This perspective covers recent developments in the de novo synthesis of aromatic heterocycles via palladium-catalysed α-arylation reactions of carbonyls, which is itself a powerful transformation that has undergone significant development in recent years. |
format | Online Article Text |
id | pubmed-4424829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-44248292015-05-13 Palladium-catalyzed α-arylation of carbonyls in the de novo synthesis of aromatic heterocycles Potukuchi, Harish K. Spork, Anatol P. Donohoe, Timothy J. Org Biomol Chem Chemistry Aromatic heterocycles are a very well represented motif in natural products and have found various applications in chemistry and material science, as well as being commonly found in pharmaceutical agents. Thus, new and efficient routes towards this class of compound are always desirable, particularly if they expand the scope of chemical methodology or facilitate more effective pathways to complex substitution patterns. This perspective covers recent developments in the de novo synthesis of aromatic heterocycles via palladium-catalysed α-arylation reactions of carbonyls, which is itself a powerful transformation that has undergone significant development in recent years. Royal Society of Chemistry 2015-04-21 2015-03-19 /pmc/articles/PMC4424829/ /pubmed/25789887 http://dx.doi.org/10.1039/c5ob00055f Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Potukuchi, Harish K. Spork, Anatol P. Donohoe, Timothy J. Palladium-catalyzed α-arylation of carbonyls in the de novo synthesis of aromatic heterocycles |
title | Palladium-catalyzed α-arylation of carbonyls in the de novo synthesis of aromatic heterocycles |
title_full | Palladium-catalyzed α-arylation of carbonyls in the de novo synthesis of aromatic heterocycles |
title_fullStr | Palladium-catalyzed α-arylation of carbonyls in the de novo synthesis of aromatic heterocycles |
title_full_unstemmed | Palladium-catalyzed α-arylation of carbonyls in the de novo synthesis of aromatic heterocycles |
title_short | Palladium-catalyzed α-arylation of carbonyls in the de novo synthesis of aromatic heterocycles |
title_sort | palladium-catalyzed α-arylation of carbonyls in the de novo synthesis of aromatic heterocycles |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424829/ https://www.ncbi.nlm.nih.gov/pubmed/25789887 http://dx.doi.org/10.1039/c5ob00055f |
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