Volatiles from the hypoxylaceous fungi and Hypoxylon macrocarpum.
dc.contributor.author | Rinkel, Jan | |
dc.contributor.author | Babczyk, Alexander | |
dc.contributor.author | Wang, Tao | |
dc.contributor.author | Stadler, Marc | |
dc.contributor.author | Dickschat, Jeroen S | |
dc.date.accessioned | 2019-02-01T14:10:24Z | |
dc.date.available | 2019-02-01T14:10:24Z | |
dc.date.issued | 2018-01-01 | |
dc.identifier.issn | 1860-5397 | |
dc.identifier.pmid | 30591821 | |
dc.identifier.doi | 10.3762/bjoc.14.277 | |
dc.identifier.uri | http://hdl.handle.net/10033/621675 | |
dc.description.abstract | The 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.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85059309527&origin=inward | en |
dc.rights | Attribution-NonCommercial-ShareAlike 4.0 International | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | * |
dc.subject | constitutional isomerism | en_US |
dc.subject | gas chromatography | en_US |
dc.subject | mass spectrometry | en_US |
dc.subject | natural products | en_US |
dc.subject | volatiles | en_US |
dc.title | Volatiles from the hypoxylaceous fungi and Hypoxylon macrocarpum. | en_US |
dc.type | Article | en_US |
dc.contributor.department | HZI,Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstr. 7,38124 Braunschweig, Germany. | en_US |
dc.identifier.url | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85059309527&origin=inward | en |
refterms.dateFOA | 2019-02-01T14:10:25Z | |
dc.source.journaltitle | Beilstein journal of organic chemistry |