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- Publisher Website: 10.1016/S0031-9422(01)00358-2
- Scopus: eid_2-s2.0-0035861324
- PMID: 11738400
- WOS: WOS:000172949900003
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Article: Deoxyarteannuin B, dihydro-deoxyarteannuin B and trans-5-hydroxy-2-isopropenyl-5-methylhex-3-en-1-ol from Artemisia anuua
Title | Deoxyarteannuin B, dihydro-deoxyarteannuin B and trans-5-hydroxy-2-isopropenyl-5-methylhex-3-en-1-ol from Artemisia anuua |
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Authors | |
Keywords | 2D-NMR Artemisia annua L. Compositae Deoxyarteannuin B Dihydro-deoxyarteannuin B Epi-deoxyarteannuin B Isoannulide Monoterpene Sesquiterpene Trans-5-Hydroxy-2-isopropenyl-5-methylhex-3-en-1-ol |
Issue Date | 2001 |
Publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/phytochem |
Citation | Phytochemistry, 2001, v. 58 n. 8, p. 1159-1166 How to Cite? |
Abstract | The amorphane sesquiterpenes, deoxyarteannuin B and dihydro-deoxyarteannuin B, were isolated from Artemisia annua and their structures mainly determined by two-dimensional NMR spectoscopic analyses. The irregular monoterpene, trans-5-hydroxy-2-isopropenyl-5-methylhex-3-en-1-ol, was also characterized in the same way, and its structure was confirmed by synthesis from lavandulol. All of these natural products are suggested to be formed by autoxidation reactions. Full assignments of the 1H and 13C resonances for the known natural products epi-deoxyarteannuin B and isoannulide, determined by the same methodology, are also reported. © 2001 Elsevier Science Ltd. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/167707 |
ISSN | 2023 Impact Factor: 3.2 2023 SCImago Journal Rankings: 0.667 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Sy, LK | en_US |
dc.contributor.author | Brown, GD | en_US |
dc.date.accessioned | 2012-10-08T03:10:16Z | - |
dc.date.available | 2012-10-08T03:10:16Z | - |
dc.date.issued | 2001 | en_US |
dc.identifier.citation | Phytochemistry, 2001, v. 58 n. 8, p. 1159-1166 | en_US |
dc.identifier.issn | 0031-9422 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/167707 | - |
dc.description.abstract | The amorphane sesquiterpenes, deoxyarteannuin B and dihydro-deoxyarteannuin B, were isolated from Artemisia annua and their structures mainly determined by two-dimensional NMR spectoscopic analyses. The irregular monoterpene, trans-5-hydroxy-2-isopropenyl-5-methylhex-3-en-1-ol, was also characterized in the same way, and its structure was confirmed by synthesis from lavandulol. All of these natural products are suggested to be formed by autoxidation reactions. Full assignments of the 1H and 13C resonances for the known natural products epi-deoxyarteannuin B and isoannulide, determined by the same methodology, are also reported. © 2001 Elsevier Science Ltd. All rights reserved. | en_US |
dc.language | eng | en_US |
dc.publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/phytochem | en_US |
dc.relation.ispartof | Phytochemistry | en_US |
dc.subject | 2D-NMR | - |
dc.subject | Artemisia annua L. | - |
dc.subject | Compositae | - |
dc.subject | Deoxyarteannuin B | - |
dc.subject | Dihydro-deoxyarteannuin B | - |
dc.subject | Epi-deoxyarteannuin B | - |
dc.subject | Isoannulide | - |
dc.subject | Monoterpene | - |
dc.subject | Sesquiterpene | - |
dc.subject | Trans-5-Hydroxy-2-isopropenyl-5-methylhex-3-en-1-ol | - |
dc.subject.mesh | Artemisia - Chemistry | en_US |
dc.subject.mesh | Artemisinins | en_US |
dc.subject.mesh | Monoterpenes | en_US |
dc.subject.mesh | Sesquiterpenes - Chemistry - Isolation & Purification | en_US |
dc.subject.mesh | Terpenes - Chemistry - Isolation & Purification | en_US |
dc.title | Deoxyarteannuin B, dihydro-deoxyarteannuin B and trans-5-hydroxy-2-isopropenyl-5-methylhex-3-en-1-ol from Artemisia anuua | en_US |
dc.type | Article | en_US |
dc.identifier.email | Sy, LK:sylk@hkucc.hku.hk | en_US |
dc.identifier.authority | Sy, LK=rp00784 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/S0031-9422(01)00358-2 | en_US |
dc.identifier.pmid | 11738400 | - |
dc.identifier.scopus | eid_2-s2.0-0035861324 | en_US |
dc.identifier.hkuros | 69025 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0035861324&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 58 | en_US |
dc.identifier.issue | 8 | en_US |
dc.identifier.spage | 1159 | en_US |
dc.identifier.epage | 1166 | en_US |
dc.identifier.isi | WOS:000172949900003 | - |
dc.publisher.place | United Kingdom | en_US |
dc.identifier.scopusauthorid | Sy, LK=35874602700 | en_US |
dc.identifier.scopusauthorid | Brown, GD=7406468149 | en_US |
dc.identifier.issnl | 0031-9422 | - |