Contiguous Quaternary Carbons : A Selection of Total Syntheses

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dc.identifier.uri http://dx.doi.org/10.15488/10553
dc.identifier.uri https://www.repo.uni-hannover.de/handle/123456789/10630
dc.contributor.author Eggert, Alina
dc.contributor.author Etling, Christoph
dc.contributor.author Lübken, Dennis
dc.contributor.author Saxarra, Marius
dc.contributor.author Kalesse, Markus
dc.date.accessioned 2021-03-17T13:48:22Z
dc.date.available 2021-03-17T13:48:22Z
dc.date.issued 2020
dc.identifier.citation Eggert, A.; Etling, C.; Lübken, D.; Saxarra, M.; Kalesse, M.: Contiguous Quaternary Carbons : A Selection of Total Syntheses. In: Molecules 25 (2020), Nr. 17, 3841. DOI: https://doi.org/10.3390/molecules25173841
dc.description.abstract 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. © 2020 by the authors. eng
dc.language.iso eng
dc.publisher Basel : MDPI AG
dc.relation.ispartofseries Molecules 25 (2020), Nr. 17
dc.rights CC BY 4.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by/4.0/
dc.subject Canataxpropellane eng
dc.subject Natural products eng
dc.subject Ortho-photo-cycloaddition eng
dc.subject Taxane diterpene eng
dc.subject Total synthesis eng
dc.subject Waihoensene eng
dc.subject.ddc 540 | Chemie ger
dc.title Contiguous Quaternary Carbons : A Selection of Total Syntheses
dc.type Article
dc.type Text
dc.relation.essn 1420-3049
dc.relation.doi https://doi.org/10.3390/molecules25173841
dc.bibliographicCitation.issue 17
dc.bibliographicCitation.volume 25
dc.bibliographicCitation.firstPage 3841
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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