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Complete 1 H and 13 C NMR assignments of aurasperone A and fonsecinone A, two bis‐naphthopyrones produced by Aspergillus aculeatus
Complete assignments of 1 H and 13 C NMR chemical shifts of the polyketides aurasperone A and fonsecinone A were made by means of nuclear Overhauser enhancement and heteronuclear NMR correlation experiments. These compounds were isolated for the first time from Aspergillus aculeatus , an endophytic...
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Published in: | Magnetic resonance in chemistry 2005-11, Vol.43 (11), p.962-965 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Complete assignments of
1
H and
13
C NMR chemical shifts of the polyketides aurasperone A and fonsecinone A were made by means of nuclear Overhauser enhancement and heteronuclear NMR correlation experiments. These compounds were isolated for the first time from
Aspergillus aculeatus
, an endophytic fungus obtained from leaves of
Melia azedarach
(Meliaceae). Copyright © 2005 John Wiley & Sons, Ltd. |
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ISSN: | 0749-1581 1097-458X |
DOI: | 10.1002/mrc.1654 |