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Pseudo five-component synthesis of 2,5-di(hetero)arylthiophenes via a one-pot Sonogashira–Glaser cyclization sequence

Based upon a consecutive one-pot Sonogashira–Glaser coupling–cyclization sequence a variety of 2,5-di(hetero)arylthiophenes were synthesized in moderate to good yields. A single Pd/Cu-catalyst system, without further catalyst addition, and easily available, stable starting materials were used, resul...

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Detalles Bibliográficos
Autores principales: Urselmann, Dominik, Antovic, Dragutin, Müller, Thomas J J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3252849/
https://www.ncbi.nlm.nih.gov/pubmed/22238523
http://dx.doi.org/10.3762/bjoc.7.174
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author Urselmann, Dominik
Antovic, Dragutin
Müller, Thomas J J
author_facet Urselmann, Dominik
Antovic, Dragutin
Müller, Thomas J J
author_sort Urselmann, Dominik
collection PubMed
description Based upon a consecutive one-pot Sonogashira–Glaser coupling–cyclization sequence a variety of 2,5-di(hetero)arylthiophenes were synthesized in moderate to good yields. A single Pd/Cu-catalyst system, without further catalyst addition, and easily available, stable starting materials were used, resulting in a concise and highly efficient route for the synthesis of the title compounds. This novel pseudo five-component synthesis starting from iodo(hetero)arenes is particularly suitable as a direct access to well-defined thiophene oligomers, which are of peculiar interest in materials science.
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spelling pubmed-32528492012-01-11 Pseudo five-component synthesis of 2,5-di(hetero)arylthiophenes via a one-pot Sonogashira–Glaser cyclization sequence Urselmann, Dominik Antovic, Dragutin Müller, Thomas J J Beilstein J Org Chem Full Research Paper Based upon a consecutive one-pot Sonogashira–Glaser coupling–cyclization sequence a variety of 2,5-di(hetero)arylthiophenes were synthesized in moderate to good yields. A single Pd/Cu-catalyst system, without further catalyst addition, and easily available, stable starting materials were used, resulting in a concise and highly efficient route for the synthesis of the title compounds. This novel pseudo five-component synthesis starting from iodo(hetero)arenes is particularly suitable as a direct access to well-defined thiophene oligomers, which are of peculiar interest in materials science. Beilstein-Institut 2011-11-04 /pmc/articles/PMC3252849/ /pubmed/22238523 http://dx.doi.org/10.3762/bjoc.7.174 Text en Copyright © 2011, Urselmann 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
Urselmann, Dominik
Antovic, Dragutin
Müller, Thomas J J
Pseudo five-component synthesis of 2,5-di(hetero)arylthiophenes via a one-pot Sonogashira–Glaser cyclization sequence
title Pseudo five-component synthesis of 2,5-di(hetero)arylthiophenes via a one-pot Sonogashira–Glaser cyclization sequence
title_full Pseudo five-component synthesis of 2,5-di(hetero)arylthiophenes via a one-pot Sonogashira–Glaser cyclization sequence
title_fullStr Pseudo five-component synthesis of 2,5-di(hetero)arylthiophenes via a one-pot Sonogashira–Glaser cyclization sequence
title_full_unstemmed Pseudo five-component synthesis of 2,5-di(hetero)arylthiophenes via a one-pot Sonogashira–Glaser cyclization sequence
title_short Pseudo five-component synthesis of 2,5-di(hetero)arylthiophenes via a one-pot Sonogashira–Glaser cyclization sequence
title_sort pseudo five-component synthesis of 2,5-di(hetero)arylthiophenes via a one-pot sonogashira–glaser cyclization sequence
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3252849/
https://www.ncbi.nlm.nih.gov/pubmed/22238523
http://dx.doi.org/10.3762/bjoc.7.174
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