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  Synthesis of positional isomeric phenylphenalenones

Ospina, F., Ramirez, A., Cano, M., Hidalgo, W., Schneider, B., & Otálvaro, F. (2017). Synthesis of positional isomeric phenylphenalenones. The Journal of Organic Chemistry, 82(7), 3873-3879. doi:10.1021/acs.joc.6b02985.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-002C-D537-D Version Permalink: https://hdl.handle.net/11858/00-001M-0000-002D-332F-8
Genre: Journal Article

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 Creators:
Ospina, F., Author
Ramirez, A., Author
Cano, M., Author
Hidalgo, William1, 2, Author           
Schneider, Bernd3, Author           
Otálvaro, F., Author
Affiliations:
1Research Group Biosynthesis / NMR, MPI for Chemical Ecology, Max Planck Society, 421898              
2IMPRS on Ecological Interactions, MPI for Chemical Ecology, Max Planck Society, Jena, DE, ou_421900              
3Research Group Biosynthesis / NMR, MPI for Chemical Ecology, Max Planck Society, ou_421898              

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 Abstract: A series of isomeric phenylphenalenones in which the phenyl ring is located at all possible peripheral positions of the phenalenone nuclei was synthesized. The structural characteristics of the series, in which topological variation is permitted with minimal electronic disturbance, could, in principle, allow for easy pharmacophore recognition when the compounds are aligned in steroidomimetic conformations.

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 Dates: 20172017-03-27
 Publication Status: Published online
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 Identifiers: Other: NMR240
DOI: 10.1021/acs.joc.6b02985
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Title: The Journal of Organic Chemistry
  Other : J. Org. Chem.
Source Genre: Journal
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Publ. Info: Washington, D.C. : American Chemical Society
Pages: - Volume / Issue: 82 (7) Sequence Number: - Start / End Page: 3873 - 3879 Identifier: ISSN: 0022-3263
CoNE: https://pure.mpg.de/cone/journals/resource/954925416967_1