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Copper(I) Catalyzed Decarboxylative Synthesis of Diareno[a,e]cyclooctatetraenes
[Image: see text] Diareno[a,e]cyclooctatetraenes find widespread applications as building blocks, ligands, and responsive cores in topologically switchable materials. However, current synthetic methods to these structures suffer from low yields or operational disadvantages. Here, we describe a pract...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490866/ https://www.ncbi.nlm.nih.gov/pubmed/35587005 http://dx.doi.org/10.1021/acs.joc.2c00286 |
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author | Tasić, Magdalena Ruiz-Soriano, Albert Strand, Daniel |
author_facet | Tasić, Magdalena Ruiz-Soriano, Albert Strand, Daniel |
author_sort | Tasić, Magdalena |
collection | PubMed |
description | [Image: see text] Diareno[a,e]cyclooctatetraenes find widespread applications as building blocks, ligands, and responsive cores in topologically switchable materials. However, current synthetic methods to these structures suffer from low yields or operational disadvantages. Here, we describe a practical three-step approach to diareno[a,e]cyclooctatetraenes using an efficient copper(I) catalyzed double decarboxylation as the key step. The sequence relies on cheap and abundant reagents, is readily performed on scale, and is amenable also to unsymmetrical derivatives that expand the utility of this intriguing class of structures. |
format | Online Article Text |
id | pubmed-9490866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94908662022-09-22 Copper(I) Catalyzed Decarboxylative Synthesis of Diareno[a,e]cyclooctatetraenes Tasić, Magdalena Ruiz-Soriano, Albert Strand, Daniel J Org Chem [Image: see text] Diareno[a,e]cyclooctatetraenes find widespread applications as building blocks, ligands, and responsive cores in topologically switchable materials. However, current synthetic methods to these structures suffer from low yields or operational disadvantages. Here, we describe a practical three-step approach to diareno[a,e]cyclooctatetraenes using an efficient copper(I) catalyzed double decarboxylation as the key step. The sequence relies on cheap and abundant reagents, is readily performed on scale, and is amenable also to unsymmetrical derivatives that expand the utility of this intriguing class of structures. American Chemical Society 2022-05-19 2022-06-03 /pmc/articles/PMC9490866/ /pubmed/35587005 http://dx.doi.org/10.1021/acs.joc.2c00286 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Tasić, Magdalena Ruiz-Soriano, Albert Strand, Daniel Copper(I) Catalyzed Decarboxylative Synthesis of Diareno[a,e]cyclooctatetraenes |
title | Copper(I) Catalyzed
Decarboxylative Synthesis of Diareno[a,e]cyclooctatetraenes |
title_full | Copper(I) Catalyzed
Decarboxylative Synthesis of Diareno[a,e]cyclooctatetraenes |
title_fullStr | Copper(I) Catalyzed
Decarboxylative Synthesis of Diareno[a,e]cyclooctatetraenes |
title_full_unstemmed | Copper(I) Catalyzed
Decarboxylative Synthesis of Diareno[a,e]cyclooctatetraenes |
title_short | Copper(I) Catalyzed
Decarboxylative Synthesis of Diareno[a,e]cyclooctatetraenes |
title_sort | copper(i) catalyzed
decarboxylative synthesis of diareno[a,e]cyclooctatetraenes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490866/ https://www.ncbi.nlm.nih.gov/pubmed/35587005 http://dx.doi.org/10.1021/acs.joc.2c00286 |
work_keys_str_mv | AT tasicmagdalena coppericatalyzeddecarboxylativesynthesisofdiarenoaecyclooctatetraenes AT ruizsorianoalbert coppericatalyzeddecarboxylativesynthesisofdiarenoaecyclooctatetraenes AT stranddaniel coppericatalyzeddecarboxylativesynthesisofdiarenoaecyclooctatetraenes |