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Article: Palladium-catalyzed decarboxylative coupling of isatoic anhydrides with arylboronic acids

TitlePalladium-catalyzed decarboxylative coupling of isatoic anhydrides with arylboronic acids
Authors
Lu, WChen, JLiu, MDing, JGao, WWu, H
Issue Date2011
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html
Citation
Organic Letters, 2011, v. 13 n. 22, p. 6114-6117 How to Cite?
DOI: http://dx.doi.org/10.1021/ol202609a
AbstractThe decarboxylative coupling of isatoic anhydrides with arylboronic acids was realized for the first time in the presence of Pd 2(dba) 3 and DPEphos, achieving aryl o-aminobenzoates with yields ranging from moderate to good. The efficiency of this procedure was demonstrated by good compatibility with fluoro, chloro, bromo, nitro, cyano, trifluoromethyl, formacyl, acetyl, thienyl, and naphthyl groups. Preliminary mechanistic experiments using deuterium labeling showed that the oxygen atom was derived from dioxygen. © 2011 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/168584
ISSN
1523-7060
2023 Impact Factor: 4.9
2023 SCImago Journal Rankings: 1.245
ISI Accession Number ID
WOS:000296756600046
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorLu, Wen_US
dc.contributor.authorChen, Jen_US
dc.contributor.authorLiu, Men_US
dc.contributor.authorDing, Jen_US
dc.contributor.authorGao, Wen_US
dc.contributor.authorWu, Hen_US
dc.date.accessioned2012-10-08T03:21:06Z-
dc.date.available2012-10-08T03:21:06Z-
dc.date.issued2011en_US
dc.identifier.citationOrganic Letters, 2011, v. 13 n. 22, p. 6114-6117en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://hdl.handle.net/10722/168584-
dc.description.abstractThe decarboxylative coupling of isatoic anhydrides with arylboronic acids was realized for the first time in the presence of Pd 2(dba) 3 and DPEphos, achieving aryl o-aminobenzoates with yields ranging from moderate to good. The efficiency of this procedure was demonstrated by good compatibility with fluoro, chloro, bromo, nitro, cyano, trifluoromethyl, formacyl, acetyl, thienyl, and naphthyl groups. Preliminary mechanistic experiments using deuterium labeling showed that the oxygen atom was derived from dioxygen. © 2011 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.subject.meshAlkylationen_US
dc.subject.meshBoronic Acids - Chemistryen_US
dc.subject.meshCarboxylic Acids - Chemistryen_US
dc.subject.meshCatalysisen_US
dc.subject.meshMolecular Structureen_US
dc.subject.meshOxazines - Chemistryen_US
dc.subject.meshOxygen - Chemistryen_US
dc.subject.meshPalladium - Chemistryen_US
dc.titlePalladium-catalyzed decarboxylative coupling of isatoic anhydrides with arylboronic acidsen_US
dc.typeArticleen_US
dc.identifier.emailLu, W:luwei@hku.hken_US
dc.identifier.authorityLu, W=rp00754en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1021/ol202609aen_US
dc.identifier.pmid22013883-
dc.identifier.scopuseid_2-s2.0-80955133311en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-80955133311&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume13en_US
dc.identifier.issue22en_US
dc.identifier.spage6114en_US
dc.identifier.epage6117en_US
dc.identifier.isiWOS:000296756600046-
dc.publisher.placeUnited Statesen_US
dc.identifier.scopusauthoridLu, W=27868087600en_US
dc.identifier.scopusauthoridChen, J=12798105400en_US
dc.identifier.scopusauthoridLiu, M=7406298559en_US
dc.identifier.scopusauthoridDing, J=8420084800en_US
dc.identifier.scopusauthoridGao, W=35299177700en_US
dc.identifier.scopusauthoridWu, H=35301460100en_US
dc.identifier.citeulike10074918-
dc.identifier.issnl1523-7052-

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