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Article: Amidation of silyl enol ethers and cholesteryl acetates with chiral ruthenium(II) schiff-base catalysts: catalytic and enantioselective studies.

TitleAmidation of silyl enol ethers and cholesteryl acetates with chiral ruthenium(II) schiff-base catalysts: catalytic and enantioselective studies.
Authors
Liang, JLYu, XQChe, CM
Issue Date2002
PublisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/Publishing/Journals/cc/index.asp
Citation
Chemical Communications (Cambridge, England), 2002 n. 2, p. 124-125 How to Cite?
DOI: http://dx.doi.org/10.1039/B109272C
AbstractChiral ruthenium(II)-salen complexes [RuII(salen)(PPh3)2] catalyse asymmetric aziridination of alkenes with up to 83% ees, asymmetric amidation of silyl enol ethers with up to 97% ees, and allylic amidation of cholesteryl acetates with good regioselectivity.
Persistent Identifierhttp://hdl.handle.net/10722/167762
ISSN
1359-7345
2021 Impact Factor: 6.065
2020 SCImago Journal Rankings: 1.837
ISI Accession Number ID
WOS:000173465900008

 

DC FieldValueLanguage
dc.contributor.authorLiang, JLen_US
dc.contributor.authorYu, XQen_US
dc.contributor.authorChe, CMen_US
dc.date.accessioned2012-10-08T03:11:08Z-
dc.date.available2012-10-08T03:11:08Z-
dc.date.issued2002en_US
dc.identifier.citationChemical Communications (Cambridge, England), 2002 n. 2, p. 124-125en_US
dc.identifier.issn1359-7345en_US
dc.identifier.urihttp://hdl.handle.net/10722/167762-
dc.description.abstractChiral ruthenium(II)-salen complexes [RuII(salen)(PPh3)2] catalyse asymmetric aziridination of alkenes with up to 83% ees, asymmetric amidation of silyl enol ethers with up to 97% ees, and allylic amidation of cholesteryl acetates with good regioselectivity.en_US
dc.languageengen_US
dc.publisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/Publishing/Journals/cc/index.aspen_US
dc.relation.ispartofChemical communications (Cambridge, England)en_US
dc.subject.meshAcetates - Chemistryen_US
dc.subject.meshAmides - Chemistryen_US
dc.subject.meshCatalysisen_US
dc.subject.meshCholesterol - Chemistryen_US
dc.subject.meshEthers - Chemistryen_US
dc.subject.meshRuthenium - Chemistryen_US
dc.subject.meshSchiff Bases - Chemistryen_US
dc.subject.meshStereoisomerismen_US
dc.titleAmidation of silyl enol ethers and cholesteryl acetates with chiral ruthenium(II) schiff-base catalysts: catalytic and enantioselective studies.en_US
dc.typeArticleen_US
dc.identifier.emailChe, CM:cmche@hku.hken_US
dc.identifier.authorityChe, CM=rp00670en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1039/B109272C-
dc.identifier.pmid12120334en_US
dc.identifier.scopuseid_2-s2.0-0037148195en_US
dc.identifier.hkuros72404-
dc.identifier.issue2en_US
dc.identifier.spage124en_US
dc.identifier.epage125en_US
dc.identifier.isiWOS:000173465900008-
dc.publisher.placeUnited Kingdomen_US
dc.identifier.scopusauthoridLiang, JL=7404541484en_US
dc.identifier.scopusauthoridYu, XQ=7404115847en_US
dc.identifier.scopusauthoridChe, CM=7102442791en_US
dc.identifier.issnl1359-7345-

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