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  Sesquiterpenoid constituents of the liverwort Marsupella aquatica

Adio, A. M., von Reuß, S. H., Paul, C., Muhle, H., & König, W. A. (2007). Sesquiterpenoid constituents of the liverwort Marsupella aquatica. Tetrahedron: Asymmetry, 18(10), 1245-1253. doi:10.1016/j.tetasy.2007.05.020.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-000F-C37B-F Version Permalink: https://hdl.handle.net/11858/00-001M-0000-000F-C37C-D
Genre: Journal Article

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EXT070.pdf (Publisher version), 209KB
 
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Adio, Adewale M., Author
von Reuß, Stephan H.1, Author           
Paul, Claudia, Author
Muhle, Hermann, Author
König, Wilfried A., Author
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1External Organizations, ou_persistent22              

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 Abstract: Nine new amorphane sesquiterpenoids, (+)-7 beta-hydroxyamorpha-4,11-diene, (-)-9 alpha-hydroxyamorpha-4,7(11)-diene, (-)-3 alpha-hydroxyamorpha-4,7(11)-diene, (-)-3 alpha-acetoxyamorpha-4,7(11)-diene, (-)-amorpha-4,7(11)-dien-3-one, (+)-2,8-epoxyamorpha-4,7(11)-diene, (+)-5,9-epoxyamorpha-3,7(11)-diene, (-)-2 alpha-hydroxyamorpha-4,7(11)-diene and (-)-2 beta-acetoxyamorpha-4,7(11)-diene, were isolated from the essential oil of the liverwort Marsupella aquatica, collected near Gaschurn/Montafon, Austria. The isolated compounds and their chemical transformations were investigated using enantioselective GC and extensive spectroscopic studies (HRMS, H-1, C-13 and 2D NMR). The absolute configuration of most of the isolated compounds were established by conversions to known compounds. In addition, H-1, and C-13 NMR data of (-)-myltayl-4-ene are reported for the first time. (C) 2007 Elsevier Ltd. All rights reserved.

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 Dates: 2007
 Publication Status: Issued
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 Identifiers: Other: EXT070
DOI: 10.1016/j.tetasy.2007.05.020
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Title: Tetrahedron: Asymmetry
Source Genre: Journal
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Publ. Info: Oxford : Pergamon
Pages: - Volume / Issue: 18 (10) Sequence Number: - Start / End Page: 1245 - 1253 Identifier: ISSN: 0957-4166
CoNE: https://pure.mpg.de/cone/journals/resource/954925577039