Synthesis of new pyrrole–pyridine-based ligands using an in situ Suzuki coupling method

The compounds 6-(pyrrol-2-yl)-2,2‘-bipyridine, 2-(pyrrol-2-yl)-1,10-phenanthroline and 2-(2-(N-methylbenz[d,e]imidazole)-6-(pyrrol-2-yl)-pyridine were synthesized by using an in situ generated boronic acid for the Suzuki coupling. Crystals of the products could be grown and exhibited interesting str...

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Autores principales: Böttger, Matthias, Wiegmann, Björn, Schaumburg, Steffen, Jones, Peter G, Kowalsky, Wolfgang, Johannes, Hans-Hermann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458721/
https://www.ncbi.nlm.nih.gov/pubmed/23019431
http://dx.doi.org/10.3762/bjoc.8.116
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author Böttger, Matthias
Wiegmann, Björn
Schaumburg, Steffen
Jones, Peter G
Kowalsky, Wolfgang
Johannes, Hans-Hermann
author_facet Böttger, Matthias
Wiegmann, Björn
Schaumburg, Steffen
Jones, Peter G
Kowalsky, Wolfgang
Johannes, Hans-Hermann
author_sort Böttger, Matthias
collection PubMed
description The compounds 6-(pyrrol-2-yl)-2,2‘-bipyridine, 2-(pyrrol-2-yl)-1,10-phenanthroline and 2-(2-(N-methylbenz[d,e]imidazole)-6-(pyrrol-2-yl)-pyridine were synthesized by using an in situ generated boronic acid for the Suzuki coupling. Crystals of the products could be grown and exhibited interesting structures by X-ray analysis, one of them showing a chain-like network with the adjacent molecules linked to each other via intermolecular N–H(…)N hydrogen bonds.
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spelling pubmed-34587212012-09-27 Synthesis of new pyrrole–pyridine-based ligands using an in situ Suzuki coupling method Böttger, Matthias Wiegmann, Björn Schaumburg, Steffen Jones, Peter G Kowalsky, Wolfgang Johannes, Hans-Hermann Beilstein J Org Chem Full Research Paper The compounds 6-(pyrrol-2-yl)-2,2‘-bipyridine, 2-(pyrrol-2-yl)-1,10-phenanthroline and 2-(2-(N-methylbenz[d,e]imidazole)-6-(pyrrol-2-yl)-pyridine were synthesized by using an in situ generated boronic acid for the Suzuki coupling. Crystals of the products could be grown and exhibited interesting structures by X-ray analysis, one of them showing a chain-like network with the adjacent molecules linked to each other via intermolecular N–H(…)N hydrogen bonds. Beilstein-Institut 2012-07-09 /pmc/articles/PMC3458721/ /pubmed/23019431 http://dx.doi.org/10.3762/bjoc.8.116 Text en Copyright © 2012, Böttger 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
Böttger, Matthias
Wiegmann, Björn
Schaumburg, Steffen
Jones, Peter G
Kowalsky, Wolfgang
Johannes, Hans-Hermann
Synthesis of new pyrrole–pyridine-based ligands using an in situ Suzuki coupling method
title Synthesis of new pyrrole–pyridine-based ligands using an in situ Suzuki coupling method
title_full Synthesis of new pyrrole–pyridine-based ligands using an in situ Suzuki coupling method
title_fullStr Synthesis of new pyrrole–pyridine-based ligands using an in situ Suzuki coupling method
title_full_unstemmed Synthesis of new pyrrole–pyridine-based ligands using an in situ Suzuki coupling method
title_short Synthesis of new pyrrole–pyridine-based ligands using an in situ Suzuki coupling method
title_sort synthesis of new pyrrole–pyridine-based ligands using an in situ suzuki coupling method
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458721/
https://www.ncbi.nlm.nih.gov/pubmed/23019431
http://dx.doi.org/10.3762/bjoc.8.116
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