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and the target molecule palau'amine, whereas the structures of the guanidine groups (rings C and F) are estimated and should be treated with more caution. The protonation state of the molecule in this diagram is neutral (for simplicity) but would more likely be multiply protonated in the conditions
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The experimental structure has been modified by deleting various groups and replacing them with others, according to the structural formulae in the manuscript that were validated spectroscopically. Rings A, B, D and E are present in both precursor
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molecule, C<sub>17</sub>H<sub>22</sub>ClN<sub>9</sub>O<sub>2</sub>, based on the crystal structure of precursor '''21''' from , which is available as
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This file contains additional information, probably added from the digital camera or scanner used to create or digitize it.
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entry [https://doi.org/10.1038/ncomms9731 ''Nat. Commun.'' (2015) '''6'...
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If the file has been modified from its original state, some details may not fully reflect the modified file.
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The following pages on the
English Knowledge (XXG) use this file (pages on other projects are not listed):
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Click on a date/time to view the file as it appeared at that time.
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copyrighted, dedicated to the public domain by copyright holder
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In some countries this may not be legally possible; if so:
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released into the public domain by the copyright holder
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Add a one-line explanation of what this file represents
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569:== {{int:filedesc}} == {{Information | Description =
78:(2,013 × 2,267 pixels, file size: 582 KB, MIME type:
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Commons is a freely licensed media file repository.
378:A ball-and-stick model of the palau'amine molecule
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205:in which palau'amine is encountered.
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233:and image generated in
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624:Vertical resolution
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220:Chlorine, Cl: green
173:Acta Crystallogr. B
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217:Hydrogen, H: white
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Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
