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|a DE-627
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|e rakwb
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|a eng
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|a Guo, Zhiyong
|e verfasserin
|4 aut
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|a 1H and 13C NMR assignments for two oxaphenalenones bacillosporin C and D from the mangrove endophytic fungus SBE-14
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|c 2007
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|a Text
|b txt
|2 rdacontent
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|a ohne Hilfsmittel zu benutzen
|b n
|2 rdamedia
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|2 rdacarrier
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|a Date Completed 30.07.2007
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|a Date Revised 24.11.2016
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|a published: Print
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|a Citation Status MEDLINE
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|a Copyright (c) 2007 John Wiley & Sons, Ltd.
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|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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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Carbon Isotopes
|2 NLM
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|a Heterocyclic Compounds, 4 or More Rings
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|a Phenalenes
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|a Protons
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|a bacillosporin C
|2 NLM
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|a bacillosporin D
|2 NLM
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|a phenalen-1-one
|2 NLM
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|a 548-39-0
|2 NLM
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|a Shao, Changlun
|e verfasserin
|4 aut
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|a She, Zhigang
|e verfasserin
|4 aut
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|a Cai, Xiaoling
|e verfasserin
|4 aut
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|a Liu, Fan
|e verfasserin
|4 aut
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|a Vrijimoed, L L P
|e verfasserin
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|a Lin, Yongcheng
|e verfasserin
|4 aut
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|i Enthalten in
|t Magnetic resonance in chemistry : MRC
|d 1985
|g 45(2007), 5 vom: 01. Mai, Seite 439-41
|w (DE-627)NLM098179667
|x 1097-458X
|7 nnns
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|g volume:45
|g year:2007
|g number:5
|g day:01
|g month:05
|g pages:439-41
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