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Article: Tandem conjugate reduction-aldol cyclization using stryker's reagent

TitleTandem conjugate reduction-aldol cyclization using stryker's reagent
Authors
Issue Date2001
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html
Citation
Organic Letters, 2001, v. 3 n. 12, p. 1901-1903 How to Cite?
Abstract(formula presentation) Conjugate reduction by Stryker's reagent to form copper enolates, followed by intramolecular aldol cyclization, successfully generated five- and six-membered carbocycles in one pot efficiently. This tandem reaction is generally diastereoselective and provides good yields of the β-hydroxyketones without any dehydration at low temperatures.
Persistent Identifierhttp://hdl.handle.net/10722/69642
ISSN
2015 Impact Factor: 6.732
2015 SCImago Journal Rankings: 3.187
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.accessioned2010-09-06T06:15:31Z-
dc.date.available2010-09-06T06:15:31Z-
dc.date.issued2001en_HK
dc.identifier.citationOrganic Letters, 2001, v. 3 n. 12, p. 1901-1903en_HK
dc.identifier.issn1523-7060en_HK
dc.identifier.urihttp://hdl.handle.net/10722/69642-
dc.description.abstract(formula presentation) Conjugate reduction by Stryker's reagent to form copper enolates, followed by intramolecular aldol cyclization, successfully generated five- and six-membered carbocycles in one pot efficiently. This tandem reaction is generally diastereoselective and provides good yields of the β-hydroxyketones without any dehydration at low temperatures.en_HK
dc.languageengen_HK
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.htmlen_HK
dc.relation.ispartofOrganic Lettersen_HK
dc.titleTandem conjugate reduction-aldol cyclization using stryker's reagenten_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1523-7060&volume=3&issue=12&spage=1901&epage=1903&date=2001&atitle=Tandem+Conjugate+Reduction+-+Aldol+Cyclization+Using+Stryker%27s+Reagenten_HK
dc.identifier.emailChiu, P:pchiu@hku.hken_HK
dc.identifier.authorityChiu, P=rp00680en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/ol015944nen_HK
dc.identifier.pmid11405740-
dc.identifier.scopuseid_2-s2.0-0000975755en_HK
dc.identifier.hkuros57031en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0000975755&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume3en_HK
dc.identifier.issue12en_HK
dc.identifier.spage1901en_HK
dc.identifier.epage1903en_HK
dc.identifier.isiWOS:000169247100030-
dc.publisher.placeUnited Statesen_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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