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Article: Chiral rhodium(II,II) dimers catalyzed enantioselective intramolecular aziridination of sulfonamides and carbamates

TitleChiral rhodium(II,II) dimers catalyzed enantioselective intramolecular aziridination of sulfonamides and carbamates
Authors
Issue Date2003
PublisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetlet
Citation
Tetrahedron Letters, 2003, v. 44 n. 31, p. 5917-5920 How to Cite?
AbstractThe asymmetric intramolecular aziridination of unsaturated sulfonamides and carbamates catalyzed by chiral dirhodium(II,II) complexes were achieved in good yields (up to 95%) and enantioselectivity (up to 76% e.e.). © 2003 Elsevier Ltd. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/69228
ISSN
2023 Impact Factor: 1.5
2023 SCImago Journal Rankings: 0.323
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorLiang, JLen_HK
dc.contributor.authorYuan, SXen_HK
dc.contributor.authorChan, PWHen_HK
dc.contributor.authorChe, CMen_HK
dc.date.accessioned2010-09-06T06:11:45Z-
dc.date.available2010-09-06T06:11:45Z-
dc.date.issued2003en_HK
dc.identifier.citationTetrahedron Letters, 2003, v. 44 n. 31, p. 5917-5920en_HK
dc.identifier.issn0040-4039en_HK
dc.identifier.urihttp://hdl.handle.net/10722/69228-
dc.description.abstractThe asymmetric intramolecular aziridination of unsaturated sulfonamides and carbamates catalyzed by chiral dirhodium(II,II) complexes were achieved in good yields (up to 95%) and enantioselectivity (up to 76% e.e.). © 2003 Elsevier Ltd. All rights reserved.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.titleChiral rhodium(II,II) dimers catalyzed enantioselective intramolecular aziridination of sulfonamides and carbamatesen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0040-4039&volume=44&spage=5917&epage=5920&date=2003&atitle=Chiral+rhodium(II,II)+dimers+catalyzed+enantioselective+intramolecular+aziridination+of+sulfonamides+and+carbamates+en_HK
dc.identifier.emailChe, CM:cmche@hku.hken_HK
dc.identifier.authorityChe, CM=rp00670en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/S0040-4039(03)01409-6en_HK
dc.identifier.scopuseid_2-s2.0-0037631116en_HK
dc.identifier.hkuros91564en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0037631116&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume44en_HK
dc.identifier.issue31en_HK
dc.identifier.spage5917en_HK
dc.identifier.epage5920en_HK
dc.identifier.isiWOS:000184220600036-
dc.publisher.placeUnited Kingdomen_HK
dc.identifier.scopusauthoridLiang, JL=7404541484en_HK
dc.identifier.scopusauthoridYuan, SX=7403272864en_HK
dc.identifier.scopusauthoridChan, PWH=13607033800en_HK
dc.identifier.scopusauthoridChe, CM=7102442791en_HK
dc.identifier.issnl0040-4039-

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