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Article: Oxidation of anisoles to p-benzoquinone monoketals catalyzed by a ruthenium complex of 1,4,7-trimethyl-1,4,7-triazacyclononane with tert-butyl hydroperoxide

TitleOxidation of anisoles to p-benzoquinone monoketals catalyzed by a ruthenium complex of 1,4,7-trimethyl-1,4,7-triazacyclononane with tert-butyl hydroperoxide
Authors
Cheung, WHYip, WPYu, WYChe, CM
KeywordsOxidation
Quinones
Ruthenium catalyst
Tert-butyl hydroperoxide
Issue Date2005
PublisherN R C Research Press. The Journal's web site is located at http://pubs.nrc-cnrc.gc.ca/cgi-bin/rp/rp2_desc_e?cjc
Citation
Canadian Journal Of Chemistry, 2005, v. 83 n. 6-7, p. 521-526 How to Cite?
DOI: http://dx.doi.org/10.1139/v05-060
AbstractA protocol based on [RuIII(Me3tacn)(CF 3CO2)2(H2O)]CF3CO 2 (1, Me3tacn = 1,4,7-trimethyl-1,4,7-triazacyclononane) as catalyst and tert-butyl hydroperoxide (TBHP) as oxidant was developed for oxidation of anisoles to p-benzoquinone monoketals. This reaction can be formally considered as regioselective aromatic C-H oxidation. With 2-methoxyanisole as substrate, 3,4-dimethoxy-4-tert-butoxy-2,5-cyclohexadienone can be obtained in up to 82% yield based on 84% substrate conversion. © 2005 NRC Canada.
Persistent Identifierhttp://hdl.handle.net/10722/44587
ISSN
0008-4042
2023 Impact Factor: 1.1
2023 SCImago Journal Rankings: 0.223
ISI Accession Number ID
WOS:000231832500003
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorCheung, WHen_HK
dc.contributor.authorYip, WPen_HK
dc.contributor.authorYu, WYen_HK
dc.contributor.authorChe, CMen_HK
dc.date.accessioned2007-10-30T06:05:10Z-
dc.date.available2007-10-30T06:05:10Z-
dc.date.issued2005en_HK
dc.identifier.citationCanadian Journal Of Chemistry, 2005, v. 83 n. 6-7, p. 521-526en_HK
dc.identifier.issn0008-4042en_HK
dc.identifier.urihttp://hdl.handle.net/10722/44587-
dc.description.abstractA protocol based on [RuIII(Me3tacn)(CF 3CO2)2(H2O)]CF3CO 2 (1, Me3tacn = 1,4,7-trimethyl-1,4,7-triazacyclononane) as catalyst and tert-butyl hydroperoxide (TBHP) as oxidant was developed for oxidation of anisoles to p-benzoquinone monoketals. This reaction can be formally considered as regioselective aromatic C-H oxidation. With 2-methoxyanisole as substrate, 3,4-dimethoxy-4-tert-butoxy-2,5-cyclohexadienone can be obtained in up to 82% yield based on 84% substrate conversion. © 2005 NRC Canada.en_HK
dc.format.extent90889 bytes-
dc.format.extent4079 bytes-
dc.format.mimetypeapplication/pdf-
dc.format.mimetypetext/plain-
dc.languageengen_HK
dc.publisherN R C Research Press. The Journal's web site is located at http://pubs.nrc-cnrc.gc.ca/cgi-bin/rp/rp2_desc_e?cjcen_HK
dc.relation.ispartofCanadian Journal of Chemistryen_HK
dc.rightsCanadian Journal of Chemistry. Copyright © N R C Research Press.en_HK
dc.subjectOxidationen_HK
dc.subjectQuinonesen_HK
dc.subjectRuthenium catalysten_HK
dc.subjectTert-butyl hydroperoxideen_HK
dc.titleOxidation of anisoles to p-benzoquinone monoketals catalyzed by a ruthenium complex of 1,4,7-trimethyl-1,4,7-triazacyclononane with tert-butyl hydroperoxideen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0008-4042&volume=83&issue=6-7&spage=521&epage=526&date=2005&atitle=Oxidation+of+anisoles+to+p-benzoquinone+monoketals+catalyzed+by+a+ruthenium+complex+of+1,4,7-trimethyl-1,4,7-triazacyclononane+with+tert-butyl+hydroperoxideen_HK
dc.identifier.emailCheung, WH: sunnycwh@hku.hken_HK
dc.identifier.emailChe, CM: cmche@hku.hken_HK
dc.identifier.authorityCheung, WH=rp00246en_HK
dc.identifier.authorityChe, CM=rp00670en_HK
dc.description.naturepublished_or_final_versionen_HK
dc.identifier.doi10.1139/v05-060en_HK
dc.identifier.scopuseid_2-s2.0-29244458335en_HK
dc.identifier.hkuros103820-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-29244458335&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume83en_HK
dc.identifier.issue6-7en_HK
dc.identifier.spage521en_HK
dc.identifier.epage526en_HK
dc.identifier.isiWOS:000231832500003-
dc.publisher.placeCanadaen_HK
dc.identifier.scopusauthoridCheung, WH=36152058800en_HK
dc.identifier.scopusauthoridYip, WP=8751048200en_HK
dc.identifier.scopusauthoridYu, WY=7403913673en_HK
dc.identifier.scopusauthoridChe, CM=7102442791en_HK
dc.identifier.issnl0008-4042-

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