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Article: A mild catalytic oxidation system: Ruthenium porphyrin and 2,6-dichloropyridine n-oxide applied for alkene dihydroxylation

TitleA mild catalytic oxidation system: Ruthenium porphyrin and 2,6-dichloropyridine n-oxide applied for alkene dihydroxylation
Authors
Keywords2,6-dichloropyridine N-oxide
alkenes
catalytic oxidation
dihydroxylation
ruthenium porphyrin
Issue Date2010
PublisherWiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=1615-4150
Citation
Advanced Synthesis And Catalysis, 2010, v. 352 n. 18, p. 3190-3194 How to Cite?
AbstractA new method was developed to transform alkenes into three types of functional molecules, including epoxides, aldehydes and 1,2-diols by using dichlororuthenium(IV) meso-tetrakis(2,6-dichlorophenyl)porphyrin [Ru(IV)(TDCPP)Cl 2] as catalyst and 2,6-dichloropyridine N-oxide (Cl 2pyNO) as the oxidant, in which the 1,2-diols were afforded via "one-pot" reactions in moderate yields. Copyright © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Persistent Identifierhttp://hdl.handle.net/10722/134348
ISSN
2015 Impact Factor: 6.453
2015 SCImago Journal Rankings: 2.729
ISI Accession Number ID
Funding AgencyGrant Number
National Nature Science Foundation of China20872095
20802023
University Grants Council of HKSARAoE 10/01P
Hong Kong Research Grants CouncilHKU 1/CRF/08
Funding Information:

This work was supported by the National Nature Science Foundation of China (Nos. 20872095 and 20802023), University Grants Council of HKSAR (the Area of Excellence Scheme: AoE 10/01P), and the Hong Kong Research Grants Council (HKU 1/CRF/08).

References

 

DC FieldValueLanguage
dc.contributor.authorHu, WXen_HK
dc.contributor.authorLi, PRen_HK
dc.contributor.authorJiang, Gen_HK
dc.contributor.authorChe, CMen_HK
dc.contributor.authorChen, Jen_HK
dc.date.accessioned2011-06-17T09:18:27Z-
dc.date.available2011-06-17T09:18:27Z-
dc.date.issued2010en_HK
dc.identifier.citationAdvanced Synthesis And Catalysis, 2010, v. 352 n. 18, p. 3190-3194en_HK
dc.identifier.issn1615-4150en_HK
dc.identifier.urihttp://hdl.handle.net/10722/134348-
dc.description.abstractA new method was developed to transform alkenes into three types of functional molecules, including epoxides, aldehydes and 1,2-diols by using dichlororuthenium(IV) meso-tetrakis(2,6-dichlorophenyl)porphyrin [Ru(IV)(TDCPP)Cl 2] as catalyst and 2,6-dichloropyridine N-oxide (Cl 2pyNO) as the oxidant, in which the 1,2-diols were afforded via "one-pot" reactions in moderate yields. Copyright © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.en_HK
dc.languageengen_US
dc.publisherWiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=1615-4150en_HK
dc.relation.ispartofAdvanced Synthesis and Catalysisen_HK
dc.subject2,6-dichloropyridine N-oxideen_HK
dc.subjectalkenesen_HK
dc.subjectcatalytic oxidationen_HK
dc.subjectdihydroxylationen_HK
dc.subjectruthenium porphyrinen_HK
dc.titleA mild catalytic oxidation system: Ruthenium porphyrin and 2,6-dichloropyridine n-oxide applied for alkene dihydroxylationen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1615-4150&volume=352&issue=18&spage=3190&epage=3194&date=2010&atitle=A+mild+catalytic+oxidation+system:+ruthenium+porphyrin+and+2,6-dichloropyridine+n-oxide+applied+for+alkene+dihydroxylation-
dc.identifier.emailChe, CM:cmche@hku.hken_HK
dc.identifier.authorityChe, CM=rp00670en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/adsc.201000455en_HK
dc.identifier.scopuseid_2-s2.0-78650357218en_HK
dc.identifier.hkuros185597en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-78650357218&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume352en_HK
dc.identifier.issue18en_HK
dc.identifier.spage3190en_HK
dc.identifier.epage3194en_HK
dc.identifier.isiWOS:000285397800017-
dc.publisher.placeGermanyen_HK
dc.identifier.scopusauthoridHu, WX=7404360030en_HK
dc.identifier.scopusauthoridLi, PR=8422643700en_HK
dc.identifier.scopusauthoridJiang, G=24923040500en_HK
dc.identifier.scopusauthoridChe, CM=7102442791en_HK
dc.identifier.scopusauthoridChen, J=36681840300en_HK

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