New cadinane sesquiterpenoids from the basidiomycetous fungus Pholiota sp.Electronic supplementary information (ESI) available: Experimental procedures, NMR spectra of compounds 1-5. CCDC 861573 and 861574. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6ra22448b

Five new cadinane sesquiterpenoids, pholiotins A-E ( 1-5 ), and three known compounds, 11-hydroxy-1(10)-valencen-2-one ( 6 ), 8,11-dihydroxy-1(10)-eremophilen-2-one ( 7 ) and durgamone ( 8 ), were isolated from the crude extract of Pholiota sp. Their structures were established on the basis of exten...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Lin, Jie, Wang, Renlei, Xu, Guohua, Ding, Zhengfeng, Zhu, Xueshen, Liu, Xingzhong, Zou, Jian, Chen, Guodong, Li, Li, Liu, Ling
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Five new cadinane sesquiterpenoids, pholiotins A-E ( 1-5 ), and three known compounds, 11-hydroxy-1(10)-valencen-2-one ( 6 ), 8,11-dihydroxy-1(10)-eremophilen-2-one ( 7 ) and durgamone ( 8 ), were isolated from the crude extract of Pholiota sp. Their structures were established on the basis of extensive spectroscopic analysis. Their absolute configurations were determined by X-ray diffraction, the Snatzke's method and electronic circular dichroism (ECD) calculations. All isolates were tested for antifungal activity. The basidiomycetous fungus Pholiota sp. produced five new cadinane sesquiterpenoids pholiotins A-E ( 1-5 ). The absolute configurations were determined by X-ray diffraction, the Snatzke's method and electronic circular dichroism (ECD) calculations.
ISSN:2046-2069
DOI:10.1039/c6ra22448b