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Novel naphthylpyridines from cobalt-catalyzed cyclotrimerization of a chiral diyne
ABSTRACT: The concise synthesis of a novel chiral diyne substrate for the assembly of chiral naphthylpyridines was described and different conditions for the cobalt-catalyzed co-cyclotrimerization with nitriles investigated. The products are novel naphthylpyridines possessing configurationally stabl...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5906485/ https://www.ncbi.nlm.nih.gov/pubmed/29681656 http://dx.doi.org/10.1007/s00706-017-2083-9 |
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author | Trommer, Volkmar Fischer, Fabian Hapke, Marko |
author_facet | Trommer, Volkmar Fischer, Fabian Hapke, Marko |
author_sort | Trommer, Volkmar |
collection | PubMed |
description | ABSTRACT: The concise synthesis of a novel chiral diyne substrate for the assembly of chiral naphthylpyridines was described and different conditions for the cobalt-catalyzed co-cyclotrimerization with nitriles investigated. The products are novel naphthylpyridines possessing configurationally stable biaryl axes. GRAPHICAL ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00706-017-2083-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5906485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-59064852018-04-20 Novel naphthylpyridines from cobalt-catalyzed cyclotrimerization of a chiral diyne Trommer, Volkmar Fischer, Fabian Hapke, Marko Monatsh Chem Original Paper ABSTRACT: The concise synthesis of a novel chiral diyne substrate for the assembly of chiral naphthylpyridines was described and different conditions for the cobalt-catalyzed co-cyclotrimerization with nitriles investigated. The products are novel naphthylpyridines possessing configurationally stable biaryl axes. GRAPHICAL ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00706-017-2083-9) contains supplementary material, which is available to authorized users. Springer Vienna 2017-11-28 2018 /pmc/articles/PMC5906485/ /pubmed/29681656 http://dx.doi.org/10.1007/s00706-017-2083-9 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Paper Trommer, Volkmar Fischer, Fabian Hapke, Marko Novel naphthylpyridines from cobalt-catalyzed cyclotrimerization of a chiral diyne |
title | Novel naphthylpyridines from cobalt-catalyzed cyclotrimerization of a chiral diyne |
title_full | Novel naphthylpyridines from cobalt-catalyzed cyclotrimerization of a chiral diyne |
title_fullStr | Novel naphthylpyridines from cobalt-catalyzed cyclotrimerization of a chiral diyne |
title_full_unstemmed | Novel naphthylpyridines from cobalt-catalyzed cyclotrimerization of a chiral diyne |
title_short | Novel naphthylpyridines from cobalt-catalyzed cyclotrimerization of a chiral diyne |
title_sort | novel naphthylpyridines from cobalt-catalyzed cyclotrimerization of a chiral diyne |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5906485/ https://www.ncbi.nlm.nih.gov/pubmed/29681656 http://dx.doi.org/10.1007/s00706-017-2083-9 |
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