| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5222735 | Tetrahedron | 2009 | 7 Pages |
Abstract
New isolated metabolites have shed light on the detoxification mechanism of 6-pentyl-pyranone by Trichoderma spp. All new compounds were synthesized and their stereoisomers characterized. The absolute configuration of 6-[(1â²R,2â²S)-dihydroxypentyl]-2H-pyran-2-one and 6-[(1â²S,2â²R)-propyloxiran-1-yl]-2H-pyran-2-one was determined by NMR analysis of the corresponding Mosher's esters.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Mourad Daoubi, Cristina Pinedo-Rivilla, M. Belén Rubio, Rosa Hermosa, Enrique Monte, Josefina Aleu, Isidro G. Collado,