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Contiguous Quaternary Carbons: A Selection of Total Syntheses

Contiguous quaternary carbons in terpene natural products remain a major challenge in total synthesis. Synthetic strategies to overcome this challenge will be a pivotal prerequisite to the medicinal application of natural products and their analogs or derivatives. In this review, we cover syntheses...

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Autores principales: Eggert, Alina, Etling, Christoph, Lübken, Dennis, Saxarra, Marius, Kalesse, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7504199/
https://www.ncbi.nlm.nih.gov/pubmed/32847075
http://dx.doi.org/10.3390/molecules25173841
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author Eggert, Alina
Etling, Christoph
Lübken, Dennis
Saxarra, Marius
Kalesse, Markus
author_facet Eggert, Alina
Etling, Christoph
Lübken, Dennis
Saxarra, Marius
Kalesse, Markus
author_sort Eggert, Alina
collection PubMed
description Contiguous quaternary carbons in terpene natural products remain a major challenge in total synthesis. Synthetic strategies to overcome this challenge will be a pivotal prerequisite to the medicinal application of natural products and their analogs or derivatives. In this review, we cover syntheses of natural products that exhibit a dense assembly of quaternary carbons and whose syntheses were uncompleted until recently. While discussing their syntheses, we not only cover the most recent total syntheses but also provide an update on the status quo of modern syntheses of complex natural products. Herein, we review (±)-canataxpropellane, (+)-waihoensene, (–)-illisimonin A and (±)-11-O-debenzoyltashironin as prominent examples of natural products bearing contiguous quaternary carbons.
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spelling pubmed-75041992020-09-24 Contiguous Quaternary Carbons: A Selection of Total Syntheses Eggert, Alina Etling, Christoph Lübken, Dennis Saxarra, Marius Kalesse, Markus Molecules Review Contiguous quaternary carbons in terpene natural products remain a major challenge in total synthesis. Synthetic strategies to overcome this challenge will be a pivotal prerequisite to the medicinal application of natural products and their analogs or derivatives. In this review, we cover syntheses of natural products that exhibit a dense assembly of quaternary carbons and whose syntheses were uncompleted until recently. While discussing their syntheses, we not only cover the most recent total syntheses but also provide an update on the status quo of modern syntheses of complex natural products. Herein, we review (±)-canataxpropellane, (+)-waihoensene, (–)-illisimonin A and (±)-11-O-debenzoyltashironin as prominent examples of natural products bearing contiguous quaternary carbons. MDPI 2020-08-24 /pmc/articles/PMC7504199/ /pubmed/32847075 http://dx.doi.org/10.3390/molecules25173841 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Eggert, Alina
Etling, Christoph
Lübken, Dennis
Saxarra, Marius
Kalesse, Markus
Contiguous Quaternary Carbons: A Selection of Total Syntheses
title Contiguous Quaternary Carbons: A Selection of Total Syntheses
title_full Contiguous Quaternary Carbons: A Selection of Total Syntheses
title_fullStr Contiguous Quaternary Carbons: A Selection of Total Syntheses
title_full_unstemmed Contiguous Quaternary Carbons: A Selection of Total Syntheses
title_short Contiguous Quaternary Carbons: A Selection of Total Syntheses
title_sort contiguous quaternary carbons: a selection of total syntheses
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7504199/
https://www.ncbi.nlm.nih.gov/pubmed/32847075
http://dx.doi.org/10.3390/molecules25173841
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AT saxarramarius contiguousquaternarycarbonsaselectionoftotalsyntheses
AT kalessemarkus contiguousquaternarycarbonsaselectionoftotalsyntheses