Matches in UGent Biblio for { <https://biblio.ugent.be/publication/3002715#aggregation> ?p ?o. }
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- aggregation classification "C3".
- aggregation creator B133364.
- aggregation creator B133365.
- aggregation creator B133366.
- aggregation creator B133367.
- aggregation creator B133368.
- aggregation creator B133369.
- aggregation creator B133370.
- aggregation creator B133371.
- aggregation creator B133372.
- aggregation creator B133373.
- aggregation creator person.
- aggregation creator person.
- aggregation date "2012".
- aggregation hasFormat 3002715.bibtex.
- aggregation hasFormat 3002715.csv.
- aggregation hasFormat 3002715.dc.
- aggregation hasFormat 3002715.didl.
- aggregation hasFormat 3002715.doc.
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- aggregation hasFormat 3002715.txt.
- aggregation hasFormat 3002715.xls.
- aggregation hasFormat 3002715.yaml.
- aggregation language "eng".
- aggregation subject "Chemistry".
- aggregation title "On the determination of the stereochemistry of semisynthetic natural product analogues using chiroptical spectroscopy: desulfurization of epidithiodioxopiperazine fungal metabolites".
- aggregation abstract "Isolation and semisynthetic modification of the fungal metabolite chaetocin gave access to a desulfurized analogue of this natural product. Detailed chiroptical studies, comparing experimentally obtained optical rotation values, electronic circular dichroism spectra, and vibrational circular dichroism spectra to computationally simulated ones, reveal the desulfurization of chaetocin to unambiguously proceed with retention of configuration. Consideration of the plausible mechanisms for this process highlighted inconsistencies in the stereochemical assignment of related molecules in the literature. This in turn allowed the stereochemical reassignment of the natural product analogue dethiodehydrogliotoxin.".
- aggregation authorList BK341633.
- aggregation isDescribedBy 3002715.
- aggregation similarTo LU-3002715.