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Divergent Strategy in Marine Tetracyclic Meroterpenoids Synthesis
The divergent total synthesis strategy can be successfully applied to the preparation of families of natural products using a common late-stage pluripotent intermediate. This approach is a powerful tool in organic synthesis as it offers opportunities for the efficient preparation of structurally rel...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153347/ https://www.ncbi.nlm.nih.gov/pubmed/34068313 http://dx.doi.org/10.3390/md19050273 |
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author | Rosales Martínez, Antonio Rodríguez-García, Ignacio López-Martínez, Josefa L. |
author_facet | Rosales Martínez, Antonio Rodríguez-García, Ignacio López-Martínez, Josefa L. |
author_sort | Rosales Martínez, Antonio |
collection | PubMed |
description | The divergent total synthesis strategy can be successfully applied to the preparation of families of natural products using a common late-stage pluripotent intermediate. This approach is a powerful tool in organic synthesis as it offers opportunities for the efficient preparation of structurally related compounds. This article reviews the synthesis of the marine natural product aureol, as well as its use as a common intermediate in the divergent synthesis of other marine natural and non-natural tetracyclic meroterpenoids. |
format | Online Article Text |
id | pubmed-8153347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-81533472021-05-27 Divergent Strategy in Marine Tetracyclic Meroterpenoids Synthesis Rosales Martínez, Antonio Rodríguez-García, Ignacio López-Martínez, Josefa L. Mar Drugs Review The divergent total synthesis strategy can be successfully applied to the preparation of families of natural products using a common late-stage pluripotent intermediate. This approach is a powerful tool in organic synthesis as it offers opportunities for the efficient preparation of structurally related compounds. This article reviews the synthesis of the marine natural product aureol, as well as its use as a common intermediate in the divergent synthesis of other marine natural and non-natural tetracyclic meroterpenoids. MDPI 2021-05-13 /pmc/articles/PMC8153347/ /pubmed/34068313 http://dx.doi.org/10.3390/md19050273 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Rosales Martínez, Antonio Rodríguez-García, Ignacio López-Martínez, Josefa L. Divergent Strategy in Marine Tetracyclic Meroterpenoids Synthesis |
title | Divergent Strategy in Marine Tetracyclic Meroterpenoids Synthesis |
title_full | Divergent Strategy in Marine Tetracyclic Meroterpenoids Synthesis |
title_fullStr | Divergent Strategy in Marine Tetracyclic Meroterpenoids Synthesis |
title_full_unstemmed | Divergent Strategy in Marine Tetracyclic Meroterpenoids Synthesis |
title_short | Divergent Strategy in Marine Tetracyclic Meroterpenoids Synthesis |
title_sort | divergent strategy in marine tetracyclic meroterpenoids synthesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153347/ https://www.ncbi.nlm.nih.gov/pubmed/34068313 http://dx.doi.org/10.3390/md19050273 |
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