Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/122542
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dc.contributor.authorSerbian, Immo-
dc.contributor.authorCsuk, René-
dc.date.accessioned2026-03-11T07:08:23Z-
dc.date.available2026-03-11T07:08:23Z-
dc.date.issued2018-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/124488-
dc.identifier.urihttp://dx.doi.org/10.25673/122542-
dc.description.abstractThe synthesis of α- and β-amyrin was accomplished starting from easily accessible starting materials, oleanolic, and ursolic acid. The procedures allow the preparation of β-amyrin in an exceptionally short scalable manner via selective iodation and reduction. For α-amyrin, a different synthetic approach had to be chosen providing access to α-amyrin in medium-to-large scale.eng
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc540-
dc.titleAn improved scalable synthesis of α- and β-amyrineng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleMolecules-
local.bibliographicCitation.volume23-
local.bibliographicCitation.issue7-
local.bibliographicCitation.publishernameMDPI-
local.bibliographicCitation.publisherplaceBasel-
local.bibliographicCitation.doi10.3390/molecules23071552-
local.subject.keywordsα-amyrin; β-amyrin; partial synthesis-
local.openaccesstrue-
dc.identifier.ppn169087385X-
cbs.publication.displayform2018-
local.bibliographicCitation.year2018-
cbs.sru.importDate2026-03-11T07:07:50Z-
local.bibliographicCitationEnthalten in Molecules - Basel : MDPI, 1996-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

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