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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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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. |
format | Online Article Text |
id | pubmed-7178799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT alighada synthesisofthetetracyclicframeworkofpolycyclicspirolignannaturalproducts AT cunygregoryd synthesisofthetetracyclicframeworkofpolycyclicspirolignannaturalproducts |