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Article: Aziridination of alkenes with N-substituted hydrazines mediated by iodobenzene diacetate

TitleAziridination of alkenes with N-substituted hydrazines mediated by iodobenzene diacetate
Authors
Issue Date2004
PublisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetlet
Citation
Tetrahedron Letters, 2004, v. 45 n. 12, p. 2685-2688 How to Cite?
AbstractAziridination of a variety of alkenes with N-substituted hydrazines mediated by iodobenzene diacetate under mild conditions (K2CO 3, CH2Cl2) and ambient temperature were achieved in good to excellent yields (up to 99%), and conversions. The practicality and simplicity of this C-N bond formation protocol was exemplified by its application to the aziridination of cholesteryl acetate in a stereoselective manner. © 2004 Elsevier Ltd. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/69518
ISSN
2015 Impact Factor: 2.347
2015 SCImago Journal Rankings: 0.782
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorLi, Jen_HK
dc.contributor.authorLiang, JLen_HK
dc.contributor.authorChan, PWHen_HK
dc.contributor.authorChe, CMen_HK
dc.date.accessioned2010-09-06T06:14:24Z-
dc.date.available2010-09-06T06:14:24Z-
dc.date.issued2004en_HK
dc.identifier.citationTetrahedron Letters, 2004, v. 45 n. 12, p. 2685-2688en_HK
dc.identifier.issn0040-4039en_HK
dc.identifier.urihttp://hdl.handle.net/10722/69518-
dc.description.abstractAziridination of a variety of alkenes with N-substituted hydrazines mediated by iodobenzene diacetate under mild conditions (K2CO 3, CH2Cl2) and ambient temperature were achieved in good to excellent yields (up to 99%), and conversions. The practicality and simplicity of this C-N bond formation protocol was exemplified by its application to the aziridination of cholesteryl acetate in a stereoselective manner. © 2004 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.titleAziridination of alkenes with N-substituted hydrazines mediated by iodobenzene diacetateen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0040-4039&volume=45&spage=2685&epage=2688&date=2004&atitle=Aziridination+of+alkenes+with+N-substituted+hydrazines+mediated+by+iodobenzene+diacetateen_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/j.tetlet.2004.01.127en_HK
dc.identifier.scopuseid_2-s2.0-1542362197en_HK
dc.identifier.hkuros91570en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-1542362197&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume45en_HK
dc.identifier.issue12en_HK
dc.identifier.spage2685en_HK
dc.identifier.epage2688en_HK
dc.identifier.isiWOS:000220150900045-
dc.publisher.placeUnited Kingdomen_HK
dc.identifier.scopusauthoridLi, J=7410055224en_HK
dc.identifier.scopusauthoridLiang, JL=7404541484en_HK
dc.identifier.scopusauthoridChan, PWH=13607033800en_HK
dc.identifier.scopusauthoridChe, CM=7102442791en_HK

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