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Article: Chiral ruthenium-oxo complexes for enantioselective epoxidation of trans-stilbene

TitleChiral ruthenium-oxo complexes for enantioselective epoxidation of trans-stilbene
Authors
Yu, WYFung, WHZhu, JLCheung, KKHo, KKChe, CM
KeywordsAsymmetric epoxidation
Oxidation
Ruthenium
Trans-stilbene
Issue Date1999
PublisherThe Chemical Society. The Journal's web site is located at http://www.sinica.edu.tw/~ccswww/jccs.htm
Citation
Journal Of The Chinese Chemical Society, 1999, v. 46 n. 3, p. 341-349 How to Cite?
AbstractTwo oxoruthenium(IV) complexes containing C2 symmetric 1,1′-biisoquinoline (biqn) and (R,R)-3,3′-(1,2-dimethylethylenedioxy)-2,2′-bipyridine (diopy*) were prepared, and both are active oxidants for alkene epoxidations. The oxidation of styrene and cis- and trans-β-methylstyrenes by [(Cn)(diopy*)-RuIV(O)](ClO4)2 did not proceed enantioselectively, but the same oxidant can attain a moderate enantioselectivity of 33%ee for the trans-stilbene oxidation to trans-stilbene oxide. A head-on approach model, where the C=C is directed from the top to the O=Ru moiety, is proposed to account for the facial differentiation of the trans-stilbene oxidation.
Persistent Identifierhttp://hdl.handle.net/10722/69955
ISSN
0009-4536
2021 Impact Factor: 1.753
2020 SCImago Journal Rankings: 0.329
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorYu, WYen_HK
dc.contributor.authorFung, WHen_HK
dc.contributor.authorZhu, JLen_HK
dc.contributor.authorCheung, KKen_HK
dc.contributor.authorHo, KKen_HK
dc.contributor.authorChe, CMen_HK
dc.date.accessioned2010-09-06T06:18:22Z-
dc.date.available2010-09-06T06:18:22Z-
dc.date.issued1999en_HK
dc.identifier.citationJournal Of The Chinese Chemical Society, 1999, v. 46 n. 3, p. 341-349en_HK
dc.identifier.issn0009-4536en_HK
dc.identifier.urihttp://hdl.handle.net/10722/69955-
dc.description.abstractTwo oxoruthenium(IV) complexes containing C2 symmetric 1,1′-biisoquinoline (biqn) and (R,R)-3,3′-(1,2-dimethylethylenedioxy)-2,2′-bipyridine (diopy*) were prepared, and both are active oxidants for alkene epoxidations. The oxidation of styrene and cis- and trans-β-methylstyrenes by [(Cn)(diopy*)-RuIV(O)](ClO4)2 did not proceed enantioselectively, but the same oxidant can attain a moderate enantioselectivity of 33%ee for the trans-stilbene oxidation to trans-stilbene oxide. A head-on approach model, where the C=C is directed from the top to the O=Ru moiety, is proposed to account for the facial differentiation of the trans-stilbene oxidation.en_HK
dc.languageengen_HK
dc.publisherThe Chemical Society. The Journal's web site is located at http://www.sinica.edu.tw/~ccswww/jccs.htmen_HK
dc.relation.ispartofJournal of the Chinese Chemical Societyen_HK
dc.subjectAsymmetric epoxidationen_HK
dc.subjectOxidationen_HK
dc.subjectRutheniumen_HK
dc.subjectTrans-stilbeneen_HK
dc.titleChiral ruthenium-oxo complexes for enantioselective epoxidation of trans-stilbeneen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0009-4536&volume=46&spage=341&epage=349&date=1999&atitle=Chiral+ruthenium-oxo+complexes+for+enantioselective+epoxidation+of+trans-stilbeneen_HK
dc.identifier.emailChe, CM:cmche@hku.hken_HK
dc.identifier.authorityChe, CM=rp00670en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.scopuseid_2-s2.0-0008458957en_HK
dc.identifier.hkuros45934en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0008458957&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume46en_HK
dc.identifier.issue3en_HK
dc.identifier.spage341en_HK
dc.identifier.epage349en_HK
dc.publisher.placeTaiwanen_HK
dc.identifier.scopusauthoridYu, WY=7403913673en_HK
dc.identifier.scopusauthoridFung, WH=7102150303en_HK
dc.identifier.scopusauthoridZhu, JL=8362229500en_HK
dc.identifier.scopusauthoridCheung, KK=7402406613en_HK
dc.identifier.scopusauthoridHo, KK=8362229700en_HK
dc.identifier.scopusauthoridChe, CM=7102442791en_HK
dc.identifier.issnl0009-4536-

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