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Multifaceted Strategy for the Synthesis of Diverse 2,2'-Bithiophene Derivatives
New catalytically or high pressure activated reactions and routes, including coupling, double bond migration in allylic systems, and various types of cycloaddition and dihydroamination have been used for the synthesis of novel bithiophene derivatives. Thanks to the abovementioned reactions and route...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272589/ https://www.ncbi.nlm.nih.gov/pubmed/25774490 http://dx.doi.org/10.3390/molecules20034565 |
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author | Krompiec, Stanisław Filapek, Michał Grudzka-Flak, Iwona Slodek, Aneta Kula, Sławomir Malecki, Jan Grzegorz Malarz, Joanna Szafraniec-Gorol, Grażyna Penkala, Mateusz Schab-Balcerzak, Ewa Paluch, Marian Mierzwa, Michał Matussek, Marek Szlapa, Agata Pajak, Michał Blach, Dariusz Marcol, Beata Danikiewicz, Witold Boharewicz, Bartosz Iwan, Agnieszka |
author_facet | Krompiec, Stanisław Filapek, Michał Grudzka-Flak, Iwona Slodek, Aneta Kula, Sławomir Malecki, Jan Grzegorz Malarz, Joanna Szafraniec-Gorol, Grażyna Penkala, Mateusz Schab-Balcerzak, Ewa Paluch, Marian Mierzwa, Michał Matussek, Marek Szlapa, Agata Pajak, Michał Blach, Dariusz Marcol, Beata Danikiewicz, Witold Boharewicz, Bartosz Iwan, Agnieszka |
author_sort | Krompiec, Stanisław |
collection | PubMed |
description | New catalytically or high pressure activated reactions and routes, including coupling, double bond migration in allylic systems, and various types of cycloaddition and dihydroamination have been used for the synthesis of novel bithiophene derivatives. Thanks to the abovementioned reactions and routes combined with non-catalytic ones, new acetylene, butadiyne, isoxazole, 1,2,3-triazole, pyrrole, benzene, and fluoranthene derivatives with one, two or six bithiophenyl moieties have been obtained. Basic sources of crucial substrates which include bithiophene motif for catalytic reactions were 2,2'-bithiophene, gaseous acetylene and 1,3-butadiyne. |
format | Online Article Text |
id | pubmed-6272589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62725892018-12-31 Multifaceted Strategy for the Synthesis of Diverse 2,2'-Bithiophene Derivatives Krompiec, Stanisław Filapek, Michał Grudzka-Flak, Iwona Slodek, Aneta Kula, Sławomir Malecki, Jan Grzegorz Malarz, Joanna Szafraniec-Gorol, Grażyna Penkala, Mateusz Schab-Balcerzak, Ewa Paluch, Marian Mierzwa, Michał Matussek, Marek Szlapa, Agata Pajak, Michał Blach, Dariusz Marcol, Beata Danikiewicz, Witold Boharewicz, Bartosz Iwan, Agnieszka Molecules Article New catalytically or high pressure activated reactions and routes, including coupling, double bond migration in allylic systems, and various types of cycloaddition and dihydroamination have been used for the synthesis of novel bithiophene derivatives. Thanks to the abovementioned reactions and routes combined with non-catalytic ones, new acetylene, butadiyne, isoxazole, 1,2,3-triazole, pyrrole, benzene, and fluoranthene derivatives with one, two or six bithiophenyl moieties have been obtained. Basic sources of crucial substrates which include bithiophene motif for catalytic reactions were 2,2'-bithiophene, gaseous acetylene and 1,3-butadiyne. MDPI 2015-03-12 /pmc/articles/PMC6272589/ /pubmed/25774490 http://dx.doi.org/10.3390/molecules20034565 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Krompiec, Stanisław Filapek, Michał Grudzka-Flak, Iwona Slodek, Aneta Kula, Sławomir Malecki, Jan Grzegorz Malarz, Joanna Szafraniec-Gorol, Grażyna Penkala, Mateusz Schab-Balcerzak, Ewa Paluch, Marian Mierzwa, Michał Matussek, Marek Szlapa, Agata Pajak, Michał Blach, Dariusz Marcol, Beata Danikiewicz, Witold Boharewicz, Bartosz Iwan, Agnieszka Multifaceted Strategy for the Synthesis of Diverse 2,2'-Bithiophene Derivatives |
title | Multifaceted Strategy for the Synthesis of Diverse 2,2'-Bithiophene Derivatives |
title_full | Multifaceted Strategy for the Synthesis of Diverse 2,2'-Bithiophene Derivatives |
title_fullStr | Multifaceted Strategy for the Synthesis of Diverse 2,2'-Bithiophene Derivatives |
title_full_unstemmed | Multifaceted Strategy for the Synthesis of Diverse 2,2'-Bithiophene Derivatives |
title_short | Multifaceted Strategy for the Synthesis of Diverse 2,2'-Bithiophene Derivatives |
title_sort | multifaceted strategy for the synthesis of diverse 2,2'-bithiophene derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272589/ https://www.ncbi.nlm.nih.gov/pubmed/25774490 http://dx.doi.org/10.3390/molecules20034565 |
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