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Article: Aryl iodide mediated aziridination of alkenes

TitleAryl iodide mediated aziridination of alkenes
Authors
Li, JChan, PWHChe, CM
Issue Date2005
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html
Citation
Organic Letters, 2005, v. 7 n. 26, p. 5801-5804 How to Cite?
DOI: http://dx.doi.org/10.1021/ol052293c
Abstract(Chemical Equation Presented) Aryl iodide mediated aziridination of a variety of alkenes with N-aminophthalimide under mild conditions (m-CPBA, K 2CO3, CH2Cl2, 25°C) was achieved in moderate to good yields (up to 94%). By recovering the aryl iodide, a recyclable system is developed with product yield over 79% attained for the aziridination of trans-1,2-diphenylethylene. © 2005 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/167986
ISSN
1523-7060
2021 Impact Factor: 6.072
2020 SCImago Journal Rankings: 1.940
ISI Accession Number ID
WOS:000234179400014
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorLi, Jen_US
dc.contributor.authorChan, PWHen_US
dc.contributor.authorChe, CMen_US
dc.date.accessioned2012-10-08T03:13:46Z-
dc.date.available2012-10-08T03:13:46Z-
dc.date.issued2005en_US
dc.identifier.citationOrganic Letters, 2005, v. 7 n. 26, p. 5801-5804en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://hdl.handle.net/10722/167986-
dc.description.abstract(Chemical Equation Presented) Aryl iodide mediated aziridination of a variety of alkenes with N-aminophthalimide under mild conditions (m-CPBA, K 2CO3, CH2Cl2, 25°C) was achieved in moderate to good yields (up to 94%). By recovering the aryl iodide, a recyclable system is developed with product yield over 79% attained for the aziridination of trans-1,2-diphenylethylene. © 2005 American Chemical Society.en_US
dc.languageengen_US
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.htmlen_US
dc.relation.ispartofOrganic Lettersen_US
dc.titleAryl iodide mediated aziridination of alkenesen_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.doi10.1021/ol052293cen_US
dc.identifier.pmid16354070-
dc.identifier.scopuseid_2-s2.0-30144446386en_US
dc.identifier.hkuros118003-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-30144446386&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume7en_US
dc.identifier.issue26en_US
dc.identifier.spage5801en_US
dc.identifier.epage5804en_US
dc.identifier.isiWOS:000234179400014-
dc.publisher.placeUnited Statesen_US
dc.identifier.scopusauthoridLi, J=7410055224en_US
dc.identifier.scopusauthoridChan, PWH=13607033800en_US
dc.identifier.scopusauthoridChe, CM=7102442791en_US
dc.identifier.issnl1523-7052-

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