Stereochemical and Biosynthetic Rationalisation of the Tropolone Sesquiterpenoids

Li, Lei; Cox, Russell J.

dc.identifier.uri	http://dx.doi.org/10.15488/14030
dc.identifier.uri	https://www.repo.uni-hannover.de/handle/123456789/14144
dc.contributor.author	Li, Lei
dc.contributor.author	Cox, Russell J.
dc.date.accessioned	2023-06-30T05:37:19Z
dc.date.available	2023-06-30T05:37:19Z
dc.date.issued	2022
dc.identifier.citation	Li, L.; Cox, R.J.: Stereochemical and Biosynthetic Rationalisation of the Tropolone Sesquiterpenoids. In: Journal of Fungi 8 (2022), Nr. 9, 929. DOI: https://doi.org/10.3390/jof8090929
dc.description.abstract	This review summarises the known structures, biological activities, and biosynthetic pathways of the tropolone sesquiterpenoid family of fungal secondary metabolites. Synthesis of this knowledge allows likely structural and stereochemical misassignments to be revised and shows how the compounds can be divided into three main biosynthetic classes based on the stereochemistry of key biosynthetic steps.	eng
dc.language.iso	eng
dc.publisher	Basel : MDPI
dc.relation.ispartofseries	Journal of Fungi 8 (2022), Nr. 9
dc.rights	CC BY 4.0 Unported
dc.rights.uri	https://creativecommons.org/licenses/by/4.0
dc.subject	biosynthesis	eng
dc.subject	meroterpenoid	eng
dc.subject	sesquiterpenoid	eng
dc.subject	stereochemical revision	eng
dc.subject	tropolone	eng
dc.subject.ddc	570 \| Biowissenschaften, Biologie
dc.title	Stereochemical and Biosynthetic Rationalisation of the Tropolone Sesquiterpenoids	eng
dc.type	Article
dc.type	Text
dc.relation.essn	2309-608X
dc.relation.doi	https://doi.org/10.3390/jof8090929
dc.bibliographicCitation.issue	9
dc.bibliographicCitation.volume	8
dc.bibliographicCitation.firstPage	929
dc.description.version	publishedVersion
tib.accessRights	frei zug�nglich