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
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520 |a 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 
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700 1 |a She, Zhigang  |e verfasserin  |4 aut 
700 1 |a Cai, Xiaoling  |e verfasserin  |4 aut 
700 1 |a Liu, Fan  |e verfasserin  |4 aut 
700 1 |a Vrijimoed, L L P  |e verfasserin  |4 aut 
700 1 |a Lin, Yongcheng  |e verfasserin  |4 aut 
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