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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

TitleDeoxyarteannuin B, dihydro-deoxyarteannuin B and trans-5-hydroxy-2-isopropenyl-5-methylhex-3-en-1-ol from Artemisia anuua
Authors
Issue Date2001
PublisherPergamon. 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?
AbstractThe 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 Identifierhttp://hdl.handle.net/10722/167707
ISSN
2015 Impact Factor: 2.779
2015 SCImago Journal Rankings: 0.935
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorSy, LKen_US
dc.contributor.authorBrown, GDen_US
dc.date.accessioned2012-10-08T03:10:16Z-
dc.date.available2012-10-08T03:10:16Z-
dc.date.issued2001en_US
dc.identifier.citationPhytochemistry, 2001, v. 58 n. 8, p. 1159-1166en_US
dc.identifier.issn0031-9422en_US
dc.identifier.urihttp://hdl.handle.net/10722/167707-
dc.description.abstractThe 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.languageengen_US
dc.publisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/phytochemen_US
dc.relation.ispartofPhytochemistryen_US
dc.subject.meshArtemisia - Chemistryen_US
dc.subject.meshArtemisininsen_US
dc.subject.meshMonoterpenesen_US
dc.subject.meshSesquiterpenes - Chemistry - Isolation & Purificationen_US
dc.subject.meshTerpenes - Chemistry - Isolation & Purificationen_US
dc.titleDeoxyarteannuin B, dihydro-deoxyarteannuin B and trans-5-hydroxy-2-isopropenyl-5-methylhex-3-en-1-ol from Artemisia anuuaen_US
dc.typeArticleen_US
dc.identifier.emailSy, LK:sylk@hkucc.hku.hken_US
dc.identifier.authoritySy, LK=rp00784en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1016/S0031-9422(01)00358-2en_US
dc.identifier.pmid11738400-
dc.identifier.scopuseid_2-s2.0-0035861324en_US
dc.identifier.hkuros69025-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0035861324&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume58en_US
dc.identifier.issue8en_US
dc.identifier.spage1159en_US
dc.identifier.epage1166en_US
dc.identifier.isiWOS:000172949900003-
dc.publisher.placeUnited Kingdomen_US
dc.identifier.scopusauthoridSy, LK=35874602700en_US
dc.identifier.scopusauthoridBrown, GD=7406468149en_US

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