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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...

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Autores principales: Tasić, Magdalena, Ruiz-Soriano, Albert, Strand, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
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.
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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
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