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dc.contributor.author윤주영-
dc.date.accessioned2017-08-28T19:35:03Z-
dc.date.available2017-08-28T19:35:03Z-
dc.date.issued2008-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://dspace.ewha.ac.kr/handle/2015.oak/233122-
dc.description.abstract5-Substituted dipyrromethane analogues (8), (23) and (25) were synthesized by the reaction of 2-vinylpyrroles, 2-vinylthiophene or 2-vinylbenzenes with excess pyrrole in the presence of Lewis acids. Accordingly, tripyrromethane analogues could be obtained by starting with 2,5-divinyl thiophene or 2,6-divinylbenzenes. The reaction usually gave moderate yields and catalyst-dependent was seen in some cases. The reaction is compatible with other reported dipyrromethane syntheses and could be applied for the construction of unusual porphyrins. © 2008 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.titleDirect alkylation of pyrrole with vinyl substituted aromatics: versatile precursors for the synthesis of porphyrinoid macrocycles-
dc.typeArticle-
dc.relation.issue26-
dc.relation.volume49-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage4138-
dc.relation.lastpage4141-
dc.relation.journaltitleTetrahedron Letters-
dc.identifier.doi10.1016/j.tetlet.2008.04.119-
dc.identifier.wosidWOS:000256771400015-
dc.identifier.scopusid2-s2.0-44149119018-
dc.author.googleHong S.-J.-
dc.author.googleJeong S.-D.-
dc.author.googleYoo J.-
dc.author.googleKim J.S.-
dc.author.googleYoon J.-
dc.author.googleLee C.-H.-
dc.contributor.scopusid윤주영(7403587371)-
dc.date.modifydate20170601133954-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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