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dc.contributor.authorRinkel, Jan
dc.contributor.authorBabczyk, Alexander
dc.contributor.authorWang, Tao
dc.contributor.authorStadler, Marc
dc.contributor.authorDickschat, Jeroen S
dc.date.accessioned2019-02-01T14:10:24Z
dc.date.available2019-02-01T14:10:24Z
dc.date.issued2018-01-01
dc.identifier.issn1860-5397
dc.identifier.pmid30591821
dc.identifier.doi10.3762/bjoc.14.277
dc.identifier.urihttp://hdl.handle.net/10033/621675
dc.description.abstractThe volatiles emitted by the ascomycetes Hypoxylon griseobrunneum and Hypoxylon macrocarpum (Hypoxylaceae, Xylariales) were collected by use of a closed-loop stripping apparatus (CLSA) and analysed by GC-MS. The main compound class of both species were polysubstituted benzene derivatives. Their structures could only be unambiguously determined by comparison to all isomers with different substitution patterns. The substitution pattern of the main compound from H. griseobrunneum, the new natural product 2,4,5-trimethylanisole, was explainable by a polyketide biosynthesis mechanism that was supported by a feeding experiment with (methyl-2H3)methionine.en_US
dc.description.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85059309527&origin=inwarden
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subjectconstitutional isomerismen_US
dc.subjectgas chromatographyen_US
dc.subjectmass spectrometryen_US
dc.subjectnatural productsen_US
dc.subjectvolatilesen_US
dc.titleVolatiles from the hypoxylaceous fungi and Hypoxylon macrocarpum.en_US
dc.typeArticleen_US
dc.contributor.departmentHZI,Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstr. 7,38124 Braunschweig, Germany.en_US
dc.identifier.urlhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85059309527&origin=inwarden
refterms.dateFOA2019-02-01T14:10:25Z
dc.source.journaltitleBeilstein journal of organic chemistry


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