1H and 13C NMR assignments for two oxaphenalenones bacillosporin C and D from the mangrove endophytic fungus SBE-14

Copyright (c) 2007 John Wiley & Sons, Ltd.

Bibliographische Detailangaben
Veröffentlicht in:Magnetic resonance in chemistry : MRC. - 1985. - 45(2007), 5 vom: 01. Mai, Seite 439-41
1. Verfasser: Guo, Zhiyong (VerfasserIn)
Weitere Verfasser: Shao, Changlun, She, Zhigang, Cai, Xiaoling, Liu, Fan, Vrijimoed, L L P, Lin, Yongcheng
Format: Aufsatz
Sprache:English
Veröffentlicht: 2007
Zugriff auf das übergeordnete Werk:Magnetic resonance in chemistry : MRC
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Carbon Isotopes Heterocyclic Compounds, 4 or More Rings Phenalenes Protons bacillosporin C bacillosporin D phenalen-1-one 548-39-0
Beschreibung
Zusammenfassung:Copyright (c) 2007 John Wiley & Sons, Ltd.
The complete (1)H and (13)C NMR assignments are reported for the novel natural product Bacillosporin D together with the known compound Bacillosporin C. These compounds containing seven rings were isolated from the mangrove endophytic fungus SBE-14 from the South China Sea. 1D and 2D NMR experiments, including COSY, HMQC and HMBC were used to the determination of the structures and NMR assignments. It is proposed that 1 was biogenetically produced by transforming 2. Transforming a lactone to an anhydride is unusual in nature
Beschreibung:Date Completed 30.07.2007
Date Revised 24.11.2016
published: Print
Citation Status MEDLINE
ISSN:1097-458X