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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...

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Autores principales: Fingerle, Michael, Dingerkus, Juliane, Schubert, Hartmut, Wurst, Kai M., Scheele, Marcus, Bettinger, Holger F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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