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Article: Application of the tandem Stryker reduction-aldol cyclization strategy to the asymmetric synthesis of lucinone

TitleApplication of the tandem Stryker reduction-aldol cyclization strategy to the asymmetric synthesis of lucinone
Authors
Issue Date2001
PublisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetlet
Citation
Tetrahedron Letters, 2001, v. 42 n. 24, p. 4091-4093 How to Cite?
AbstractThe tandem conjugate reduction-aldol cyclization using Stryker's reagent has been employed as the key-step in an asymmetric total synthesis of lucinone. © 2001 Elsevier Science Ltd.
Persistent Identifierhttp://hdl.handle.net/10722/69686
ISSN
2015 Impact Factor: 2.347
2015 SCImago Journal Rankings: 0.782
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorChiu, Pen_HK
dc.contributor.authorSzeto, CPen_HK
dc.contributor.authorGeng, Zen_HK
dc.contributor.authorCheng, KFen_HK
dc.date.accessioned2010-09-06T06:15:55Z-
dc.date.available2010-09-06T06:15:55Z-
dc.date.issued2001en_HK
dc.identifier.citationTetrahedron Letters, 2001, v. 42 n. 24, p. 4091-4093en_HK
dc.identifier.issn0040-4039en_HK
dc.identifier.urihttp://hdl.handle.net/10722/69686-
dc.description.abstractThe tandem conjugate reduction-aldol cyclization using Stryker's reagent has been employed as the key-step in an asymmetric total synthesis of lucinone. © 2001 Elsevier Science Ltd.en_HK
dc.languageengen_HK
dc.publisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetleten_HK
dc.relation.ispartofTetrahedron Lettersen_HK
dc.titleApplication of the tandem Stryker reduction-aldol cyclization strategy to the asymmetric synthesis of lucinoneen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0040-4039&volume=42&spage=4091&epage=4093&date=2001&atitle=Application+of+the+tandem+Stryker+reduction+-+aldol+cyclization+strategy+to+the+asymmetric+synthesis+of+lucinoneen_HK
dc.identifier.emailChiu, P:pchiu@hku.hken_HK
dc.identifier.authorityChiu, P=rp00680en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/S0040-4039(01)00638-4en_HK
dc.identifier.scopuseid_2-s2.0-0035844674en_HK
dc.identifier.hkuros57033en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0035844674&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume42en_HK
dc.identifier.issue24en_HK
dc.identifier.spage4091en_HK
dc.identifier.epage4093en_HK
dc.identifier.isiWOS:000169116400033-
dc.publisher.placeUnited Kingdomen_HK
dc.identifier.scopusauthoridChiu, P=11140148700en_HK
dc.identifier.scopusauthoridSzeto, CP=7006622136en_HK
dc.identifier.scopusauthoridGeng, Z=36947090200en_HK
dc.identifier.scopusauthoridCheng, KF=7402997838en_HK

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