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dc.contributor.authorShin, JY-
dc.contributor.authorHepperle, SS-
dc.contributor.authorPatrick, BO-
dc.contributor.authorDolphin, D-
dc.date.accessioned2018-10-04T06:25:45Z-
dc.date.available2018-10-04T06:25:45Z-
dc.date.created2011-03-17-
dc.date.issued2009-07-
dc.identifier.issn1359-7345-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/92487-
dc.description.abstractalpha- and beta-tripyrrinone isomers (3-6), and a C-2 symmetric hexapyrrole (7) were isolated from the oxidation of meso-perfluorophenyl tripyrrane 1 (and meso-2,6-dichlorophenyl tripyrrane 2) with DDQ under aerobic conditions, and the structure of 3 was determined by X-ray crystallographic analysis.-
dc.languageEnglish-
dc.publisherRoyal Soc Chemistry-
dc.relation.isPartOfChemical Communications-
dc.titleOxidized Forms of a Tripyrrane: α-tripyrrinone, β-tripyrrinone and a C2 Symentric Hexapyrrole-
dc.typeArticle-
dc.identifier.doi10.1039/b901171b-
dc.type.rimsART-
dc.identifier.bibliographicCitationChemical Communications, no.17, pp.2323 - 2325-
dc.identifier.wosid000265355800018-
dc.date.tcdate2019-02-01-
dc.citation.endPage2325-
dc.citation.number17-
dc.citation.startPage2323-
dc.citation.titleChemical Communications-
dc.contributor.affiliatedAuthorShin, JY-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc14-
dc.type.docTypeArticle-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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