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Synthesis of the Tetracyclic Framework of Polycyclic Spiro Lignan Natural Products

[Image: see text] Polycyclic spiro lignans are a new family of lignan natural products recently isolated from Gymnotheca involucrata. The first synthesis of two model substrates of this rare family of natural products was achieved in six steps. An efficient strategy that features Suzuki coupling and...

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Detalles Bibliográficos
Autores principales: Ali, Ghada, Cuny, Gregory D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178799/
https://www.ncbi.nlm.nih.gov/pubmed/32337465
http://dx.doi.org/10.1021/acsomega.0c00976
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author Ali, Ghada
Cuny, Gregory D.
author_facet Ali, Ghada
Cuny, Gregory D.
author_sort Ali, Ghada
collection PubMed
description [Image: see text] Polycyclic spiro lignans are a new family of lignan natural products recently isolated from Gymnotheca involucrata. The first synthesis of two model substrates of this rare family of natural products was achieved in six steps. An efficient strategy that features Suzuki coupling and Friedel–Crafts acylation was employed to construct the ABC tricyclic fluorene framework. Subsequently, Grignard reaction followed by acid-mediated cyclization furnished the spiro cyclic ether ring D.
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spelling pubmed-71787992020-04-24 Synthesis of the Tetracyclic Framework of Polycyclic Spiro Lignan Natural Products Ali, Ghada Cuny, Gregory D. ACS Omega [Image: see text] Polycyclic spiro lignans are a new family of lignan natural products recently isolated from Gymnotheca involucrata. The first synthesis of two model substrates of this rare family of natural products was achieved in six steps. An efficient strategy that features Suzuki coupling and Friedel–Crafts acylation was employed to construct the ABC tricyclic fluorene framework. Subsequently, Grignard reaction followed by acid-mediated cyclization furnished the spiro cyclic ether ring D. American Chemical Society 2020-04-08 /pmc/articles/PMC7178799/ /pubmed/32337465 http://dx.doi.org/10.1021/acsomega.0c00976 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Ali, Ghada
Cuny, Gregory D.
Synthesis of the Tetracyclic Framework of Polycyclic Spiro Lignan Natural Products
title Synthesis of the Tetracyclic Framework of Polycyclic Spiro Lignan Natural Products
title_full Synthesis of the Tetracyclic Framework of Polycyclic Spiro Lignan Natural Products
title_fullStr Synthesis of the Tetracyclic Framework of Polycyclic Spiro Lignan Natural Products
title_full_unstemmed Synthesis of the Tetracyclic Framework of Polycyclic Spiro Lignan Natural Products
title_short Synthesis of the Tetracyclic Framework of Polycyclic Spiro Lignan Natural Products
title_sort synthesis of the tetracyclic framework of polycyclic spiro lignan natural products
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178799/
https://www.ncbi.nlm.nih.gov/pubmed/32337465
http://dx.doi.org/10.1021/acsomega.0c00976
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