Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 82, Issue 7, Pages 3873-3879Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.6b02985
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Funding
- Universidad de Antioquia
- COLCIENCIAS [111565842551]
- Max-Planck-Institut fur Chemische Okologie
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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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