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Article: Highly efficient Au(I)-catalyzed intramolecular addition of β-ketoamide to unactivated alkenes

TitleHighly efficient Au(I)-catalyzed intramolecular addition of β-ketoamide to unactivated alkenes
Authors
Issue Date2007
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/jacsat/index.html
Citation
Journal Of The American Chemical Society, 2007, v. 129 n. 18, p. 5828-5829 How to Cite?
AbstractN-Alkenyl β-ketoamides undergo cyclization in the presence of Au[P(t-Bu)2(o-biphenyl)]Cl (5 mol %) and AgOTf (5 mol %) under mild conditions with excellent regioselectivities and yields. The reaction provides an efficient method to prepare highly substituted lactams. Copyright © 2007 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/168110
ISSN
2015 Impact Factor: 13.038
2015 SCImago Journal Rankings: 7.123
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorZhou, CYen_US
dc.contributor.authorChe, CMen_US
dc.date.accessioned2012-10-08T03:15:11Z-
dc.date.available2012-10-08T03:15:11Z-
dc.date.issued2007en_US
dc.identifier.citationJournal Of The American Chemical Society, 2007, v. 129 n. 18, p. 5828-5829en_US
dc.identifier.issn0002-7863en_US
dc.identifier.urihttp://hdl.handle.net/10722/168110-
dc.description.abstractN-Alkenyl β-ketoamides undergo cyclization in the presence of Au[P(t-Bu)2(o-biphenyl)]Cl (5 mol %) and AgOTf (5 mol %) under mild conditions with excellent regioselectivities and yields. The reaction provides an efficient method to prepare highly substituted lactams. Copyright © 2007 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/jacsat/index.htmlen_US
dc.relation.ispartofJournal of the American Chemical Societyen_US
dc.subject.meshAlkenes - Chemistryen_US
dc.subject.meshAmides - Chemistryen_US
dc.subject.meshCatalysisen_US
dc.titleHighly efficient Au(I)-catalyzed intramolecular addition of β-ketoamide to unactivated alkenesen_US
dc.typeArticleen_US
dc.identifier.emailZhou, CY:cyzhou@hku.hken_US
dc.identifier.emailChe, CM:cmche@hku.hken_US
dc.identifier.authorityZhou, CY=rp00843en_US
dc.identifier.authorityChe, CM=rp00670en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1021/ja070027jen_US
dc.identifier.pmid17439216-
dc.identifier.scopuseid_2-s2.0-34248589554en_US
dc.identifier.hkuros137083-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-34248589554&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume129en_US
dc.identifier.issue18en_US
dc.identifier.spage5828en_US
dc.identifier.epage5829en_US
dc.identifier.isiWOS:000246180200022-
dc.publisher.placeUnited Statesen_US
dc.identifier.scopusauthoridZhou, CY=35742480200en_US
dc.identifier.scopusauthoridChe, CM=7102442791en_US
dc.identifier.citeulike9068404-

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