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Heteroatom Cycloaddition at the (BN)(2) Bay Region of Dibenzoperylene
Cycloaddition‐dehydration involving a BNBN‐butadiene analogue at the bay region of a dibenzoperylene and a non‐enolizable aldehyde provides a novel strategy for incorporation of the oxadiazadiborinane (B(2)N(2)CO) ring into the scaffold of a polycyclic aromatic hydrocarbon resulting in highly emissi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545313/ https://www.ncbi.nlm.nih.gov/pubmed/33798286 http://dx.doi.org/10.1002/anie.202016699 |
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author | Fingerle, Michael Dingerkus, Juliane Schubert, Hartmut Wurst, Kai M. Scheele, Marcus Bettinger, Holger F. |
author_facet | Fingerle, Michael Dingerkus, Juliane Schubert, Hartmut Wurst, Kai M. Scheele, Marcus Bettinger, Holger F. |
author_sort | Fingerle, Michael |
collection | PubMed |
description | Cycloaddition‐dehydration involving a BNBN‐butadiene analogue at the bay region of a dibenzoperylene and a non‐enolizable aldehyde provides a novel strategy for incorporation of the oxadiazadiborinane (B(2)N(2)CO) ring into the scaffold of a polycyclic aromatic hydrocarbon resulting in highly emissive compounds. |
format | Online Article Text |
id | pubmed-9545313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95453132022-10-14 Heteroatom Cycloaddition at the (BN)(2) Bay Region of Dibenzoperylene Fingerle, Michael Dingerkus, Juliane Schubert, Hartmut Wurst, Kai M. Scheele, Marcus Bettinger, Holger F. Angew Chem Int Ed Engl Communications Cycloaddition‐dehydration involving a BNBN‐butadiene analogue at the bay region of a dibenzoperylene and a non‐enolizable aldehyde provides a novel strategy for incorporation of the oxadiazadiborinane (B(2)N(2)CO) ring into the scaffold of a polycyclic aromatic hydrocarbon resulting in highly emissive compounds. John Wiley and Sons Inc. 2021-06-11 2021-07-12 /pmc/articles/PMC9545313/ /pubmed/33798286 http://dx.doi.org/10.1002/anie.202016699 Text en © 2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://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 Fingerle, Michael Dingerkus, Juliane Schubert, Hartmut Wurst, Kai M. Scheele, Marcus Bettinger, Holger F. Heteroatom Cycloaddition at the (BN)(2) Bay Region of Dibenzoperylene |
title | Heteroatom Cycloaddition at the (BN)(2) Bay Region of Dibenzoperylene |
title_full | Heteroatom Cycloaddition at the (BN)(2) Bay Region of Dibenzoperylene |
title_fullStr | Heteroatom Cycloaddition at the (BN)(2) Bay Region of Dibenzoperylene |
title_full_unstemmed | Heteroatom Cycloaddition at the (BN)(2) Bay Region of Dibenzoperylene |
title_short | Heteroatom Cycloaddition at the (BN)(2) Bay Region of Dibenzoperylene |
title_sort | heteroatom cycloaddition at the (bn)(2) bay region of dibenzoperylene |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545313/ https://www.ncbi.nlm.nih.gov/pubmed/33798286 http://dx.doi.org/10.1002/anie.202016699 |
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