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Hydroacenes Made Easy by Gold(I) Catalysis
A novel strategy for the synthesis of partially saturated acene derivatives has been developed based on a Au(I)‐catalyzed cyclization of 1,7‐enynes. This method provides straightforward access to stable polycyclic products featuring the backbone of the acene series, up to nonacene.
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5132091/ https://www.ncbi.nlm.nih.gov/pubmed/27381976 http://dx.doi.org/10.1002/anie.201604952 |
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author | Dorel, Ruth McGonigal, Paul R. Echavarren, Antonio M. |
author_facet | Dorel, Ruth McGonigal, Paul R. Echavarren, Antonio M. |
author_sort | Dorel, Ruth |
collection | PubMed |
description | A novel strategy for the synthesis of partially saturated acene derivatives has been developed based on a Au(I)‐catalyzed cyclization of 1,7‐enynes. This method provides straightforward access to stable polycyclic products featuring the backbone of the acene series, up to nonacene. |
format | Online Article Text |
id | pubmed-5132091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-51320912016-12-02 Hydroacenes Made Easy by Gold(I) Catalysis Dorel, Ruth McGonigal, Paul R. Echavarren, Antonio M. Angew Chem Int Ed Engl Communications A novel strategy for the synthesis of partially saturated acene derivatives has been developed based on a Au(I)‐catalyzed cyclization of 1,7‐enynes. This method provides straightforward access to stable polycyclic products featuring the backbone of the acene series, up to nonacene. John Wiley and Sons Inc. 2016-07-06 2016-09-05 /pmc/articles/PMC5132091/ /pubmed/27381976 http://dx.doi.org/10.1002/anie.201604952 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Communications Dorel, Ruth McGonigal, Paul R. Echavarren, Antonio M. Hydroacenes Made Easy by Gold(I) Catalysis |
title | Hydroacenes Made Easy by Gold(I) Catalysis |
title_full | Hydroacenes Made Easy by Gold(I) Catalysis |
title_fullStr | Hydroacenes Made Easy by Gold(I) Catalysis |
title_full_unstemmed | Hydroacenes Made Easy by Gold(I) Catalysis |
title_short | Hydroacenes Made Easy by Gold(I) Catalysis |
title_sort | hydroacenes made easy by gold(i) catalysis |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5132091/ https://www.ncbi.nlm.nih.gov/pubmed/27381976 http://dx.doi.org/10.1002/anie.201604952 |
work_keys_str_mv | AT dorelruth hydroacenesmadeeasybygoldicatalysis AT mcgonigalpaulr hydroacenesmadeeasybygoldicatalysis AT echavarrenantoniom hydroacenesmadeeasybygoldicatalysis |