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Monolaterol, the first configurationally assigned phenylphenalenone derivative with a stereogenic center at C-9, from Monochoria elata

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Hölscher,  D.
Department of Entomology, MPI for Chemical Ecology, Max Planck Society;

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Schneider,  B.
Research Group Biosynthesis / NMR, MPI for Chemical Ecology, Max Planck Society;

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Citation

Hölscher, D., Reichert, M., Gorls, H., Ohlenschlager, O., Bringmann, G., & Schneider, B. (2006). Monolaterol, the first configurationally assigned phenylphenalenone derivative with a stereogenic center at C-9, from Monochoria elata. Natural Product Reports, 69(11), 1614-1617. doi:10.1021/np060192x.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0012-B680-7
Abstract
Phytochemical analysis of the roots of Monochoria elata resulted in the structure elucidation of monolaterol, the first configurationally assigned phenylphenalenone-type natural product with a stereogenic center at the phenyl-bearing carbon, C-9, and fo