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Article: Mild α-halogenation reactions of 1,3-dicarbonyl compounds catalyzed by Lewis acids

TitleMild α-halogenation reactions of 1,3-dicarbonyl compounds catalyzed by Lewis acids
Authors
Issue Date2002
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/joc
Citation
Journal Of Organic Chemistry, 2002, v. 67 n. 21, p. 7429-7431 How to Cite?
AbstractLewis acid Mg(ClO4)2, combined with NBS, in CH3CN or EtOAc provided mild and fast bromination of 1,3-dicarbonyl compounds. In particular, this protocol could be applied to the α-monobromination of α-unsubstituted β-keto esters. Similar Lewis acid catalysis was also extended to the α-chlorination and iodination of 1,3-dicarbonyl compounds with NCS and NIS, respectively.
Persistent Identifierhttp://hdl.handle.net/10722/167760
ISSN
2015 Impact Factor: 4.785
2015 SCImago Journal Rankings: 2.095
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorYang, Den_US
dc.contributor.authorYan, YLen_US
dc.contributor.authorLui, Ben_US
dc.date.accessioned2012-10-08T03:11:08Z-
dc.date.available2012-10-08T03:11:08Z-
dc.date.issued2002en_US
dc.identifier.citationJournal Of Organic Chemistry, 2002, v. 67 n. 21, p. 7429-7431en_US
dc.identifier.issn0022-3263en_US
dc.identifier.urihttp://hdl.handle.net/10722/167760-
dc.description.abstractLewis acid Mg(ClO4)2, combined with NBS, in CH3CN or EtOAc provided mild and fast bromination of 1,3-dicarbonyl compounds. In particular, this protocol could be applied to the α-monobromination of α-unsubstituted β-keto esters. Similar Lewis acid catalysis was also extended to the α-chlorination and iodination of 1,3-dicarbonyl compounds with NCS and NIS, respectively.en_US
dc.languageengen_US
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/jocen_US
dc.relation.ispartofJournal of Organic Chemistryen_US
dc.titleMild α-halogenation reactions of 1,3-dicarbonyl compounds catalyzed by Lewis acidsen_US
dc.typeArticleen_US
dc.identifier.emailYang, D:yangdan@hku.hken_US
dc.identifier.authorityYang, D=rp00825en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1021/jo026025ten_US
dc.identifier.pmid12375975-
dc.identifier.scopuseid_2-s2.0-0037131155en_US
dc.identifier.hkuros75915-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0037131155&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume67en_US
dc.identifier.issue21en_US
dc.identifier.spage7429en_US
dc.identifier.epage7431en_US
dc.identifier.isiWOS:000178598600034-
dc.publisher.placeUnited Statesen_US
dc.identifier.scopusauthoridYang, D=7404800756en_US
dc.identifier.scopusauthoridYan, YL=16235517800en_US
dc.identifier.scopusauthoridLui, B=40861497100en_US
dc.identifier.citeulike9543686-

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