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dc.contributor.authorHayton, JB
dc.contributor.authorWard, BT
dc.contributor.authorElnaas, AR
dc.contributor.authorZunk, M
dc.contributor.authorHolland, DC
dc.contributor.authorMay, TW
dc.contributor.authorVoser, TM
dc.contributor.authorAbitbol, A
dc.contributor.authorCooper, O
dc.contributor.authorTiralongo, J
dc.contributor.authorGrice, ID
dc.contributor.authorCarroll, AR
dc.contributor.authorTiralongo, E
dc.date.accessioned2021-08-23T00:30:02Z
dc.date.available2021-08-23T00:30:02Z
dc.date.issued2021
dc.identifier.issn0040-4039
dc.identifier.doi10.1016/j.tetlet.2021.153294
dc.identifier.urihttp://hdl.handle.net/10072/407142
dc.description.abstractNine compounds including the new diastereomers (3′R)-fasciculic acid C (1) and (3′S)-fasciculic acid C (2), the triterpenes (3–5), the sesquiterpenes (6–7) and the diketopiperazines (8–9) were isolated from the Australian mushroom Hypholoma australianum. Several lanostane triterpenes have been isolated from the genus Hypholoma previously contain a 3-hydroxy-3-methylglutaric acid or a 3-hydroxy-3-methylglutaryl-glycine side chain. Only Hypholoma derived triterpenes possessing the S-configuration for these two side chains have been isolated previously. Compound 1 is the first example of a triterpene isolated from Hypholoma to have an R-configuration for the side chain.
dc.description.peerreviewedYes
dc.languageen
dc.publisherElsevier BV
dc.relation.ispartofpagefrom153294
dc.relation.ispartofjournalTetrahedron Letters
dc.relation.ispartofvolume78
dc.subject.fieldofresearchMedicinal and biomolecular chemistry
dc.subject.fieldofresearchMedicinal and biomolecular chemistry not elsewhere classified
dc.subject.fieldofresearchMacromolecular and materials chemistry
dc.subject.fieldofresearchOrganic chemistry
dc.subject.fieldofresearchBiochemistry and cell biology
dc.subject.fieldofresearchcode3404
dc.subject.fieldofresearchcode340499
dc.subject.fieldofresearchcode3403
dc.subject.fieldofresearchcode3405
dc.subject.fieldofresearchcode3101
dc.titleIsolation of the 3′R and 3′S diastereomers of fasciculic acid C from the Australian mushroom Hypholoma australianum
dc.typeJournal article
dc.type.descriptionC1 - Articles
dcterms.bibliographicCitationHayton, JB; Ward, BT; Elnaas, AR; Zunk, M; Holland, DC; May, TW; Voser, TM; Abitbol, A; Cooper, O; Tiralongo, J; Grice, ID; Carroll, AR; Tiralongo, E, Isolation of the 3′R and 3′S diastereomers of fasciculic acid C from the Australian mushroom Hypholoma australianum, Tetrahedron Letters, 2021, 78, pp. 153294
dc.date.updated2021-08-17T00:32:33Z
gro.hasfulltextNo Full Text
gro.griffith.authorZunk, Matthew S.
gro.griffith.authorCooper, Oren
gro.griffith.authorCarroll, Anthony R.
gro.griffith.authorTiralongo, Joe
gro.griffith.authorGrice, Darren D.


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