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dc.contributor.authorHarn, Piin-Jyeen_US
dc.contributor.authorLin, Chu-Chungen_US
dc.contributor.authorWu, Hsien-Jenen_US
dc.date.accessioned2014-12-08T15:38:20Z-
dc.date.available2014-12-08T15:38:20Z-
dc.date.issued2010-12-01en_US
dc.identifier.issn0009-4536en_US
dc.identifier.urihttp://hdl.handle.net/11536/26259-
dc.description.abstractOxidation of 3-furfurylamines 3a-e with bromine in acetone-water solution gave N-substituted 3-formylpyrroles 4a-e in good yields. A reaction mechanism via the Clauson-Kaas reaction followed by the cis-trans isomerization of the 2-ene-1,4-diones 13 and 14 was proposed to account for the formation of the pyrroles 4a-e.en_US
dc.language.isoen_USen_US
dc.subject3-Furfurylaminesen_US
dc.subject3-Formylpyrrolesen_US
dc.subjectOxidation with bromineen_US
dc.title3-Formylpyrroles from 3-Furfurylamines by Bromine Oxidation Reactionen_US
dc.typeArticleen_US
dc.identifier.journalJOURNAL OF THE CHINESE CHEMICAL SOCIETYen_US
dc.citation.volume57en_US
dc.citation.issue6Ben_US
dc.citation.spage1321en_US
dc.citation.epage1326en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000288050400016-
dc.citation.woscount1-
Appears in Collections:Articles