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

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.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0012-B680-7 Version Permalink: https://hdl.handle.net/21.11116/0000-0009-3684-5
Genre: Journal Article

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 Creators:
Hölscher, D.1, Author           
Reichert, M., Author
Gorls, H., Author
Ohlenschlager, O., Author
Bringmann, G., Author
Schneider, B.2, Author           
Affiliations:
1Department of Entomology, MPI for Chemical Ecology, Max Planck Society, ou_421895              
2Research Group Biosynthesis / NMR, MPI for Chemical Ecology, Max Planck Society, ou_421898              

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Free keywords: Gaussian-basis sets Density Vaginalis Biosynthesis Phytoalexins Exchange Fruit Agricultural Chemistry in Current Contents(R)/Agricultural, Biology & Environmental Sciences Pharmacology & Toxicology in Current Contents(R)/Life Sciences
 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

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 Dates: 2006
 Publication Status: Issued
 Pages: -
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 Rev. Type: -
 Identifiers: Other: NMR142
DOI: 10.1021/np060192x
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Title: Natural Product Reports
  Abbreviation : Nat. Prod. Rep.
Source Genre: Journal
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Publ. Info: Cambridge, England : Royal Society of Chemistry
Pages: - Volume / Issue: 69 (11) Sequence Number: - Start / End Page: 1614 - 1617 Identifier: ISSN: 0265-0568
CoNE: https://pure.mpg.de/cone/journals/resource/110978977979506