2D-NMR of natural products, part V Structure elucidation and complete1H- and13C-assignment of resin acid derivatives

1984 ◽  
Vol 115 (5) ◽  
pp. 597-603 ◽  
Author(s):  
Ernst Haslinger ◽  
Hermann Kalchhauser ◽  
Wolfgang Robien ◽  
Harald Steindl
ChemInform ◽  
2010 ◽  
Vol 23 (42) ◽  
pp. no-no
Author(s):  
ATTA-UR-RAHMAN ATTA-UR-RAHMAN ◽  
M. I. CHOUDHARY ◽  
A. PERVIN

2003 ◽  
Vol 41 (5) ◽  
pp. 359-372 ◽  
Author(s):  
Kirill A. Blinov ◽  
Dean Carlson ◽  
Mikhail E. Elyashberg ◽  
Gary E. Martin ◽  
Eduard R. Martirosian ◽  
...  

2002 ◽  
Vol 65 (5) ◽  
pp. 693-703 ◽  
Author(s):  
Mikhail E. Elyashberg ◽  
Kirill A. Blinov ◽  
Antony J. Williams ◽  
Eduard R. Martirosian ◽  
Sergey G. Molodtsov

Marine Drugs ◽  
2022 ◽  
Vol 20 (1) ◽  
pp. 43
Author(s):  
Jia-Xuan Yan ◽  
Qihao Wu ◽  
Eric J. N. Helfrich ◽  
Marc G. Chevrette ◽  
Doug R. Braun ◽  
...  

Chemical investigations of a marine sponge-associated Bacillus revealed six new imidazolium-containing compounds, bacillimidazoles A–F (1–6). Previous reports of related imidazolium-containing natural products are rare. Initially unveiled by timsTOF (trapped ion mobility spectrometry) MS data, extensive HRMS and 1D and 2D NMR analyses enabled the structural elucidation of 1–6. In addition, a plausible biosynthetic pathway to bacillimidazoles is proposed based on isotopic labeling experiments and invokes the highly reactive glycolytic adduct 2,3-butanedione. Combined, the results of structure elucidation efforts, isotopic labeling studies and bioinformatics suggest that 1–6 result from a fascinating intersection of primary and secondary metabolic pathways in Bacillus sp. WMMC1349. Antimicrobial assays revealed that, of 1–6, only compound six displayed discernible antibacterial activity, despite the close structural similarities shared by all six natural products.


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