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dc.contributor.author이상기*
dc.date.accessioned2016-08-28T12:08:53Z-
dc.date.available2016-08-28T12:08:53Z-
dc.date.issued2010*
dc.identifier.issn0040-4039*
dc.identifier.otherOAK-6316*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/220571-
dc.description.abstractTo improve the reactivity of Grubbs catalyst, novel ligands were designed and synthesized which possess nitrogen-containing heterocycles such as imidazole and pyridine. The modified catalysts were treated with a range of acids and the acid salt forms were used as catalysts for ring-closing metathesis (RCM) reactions. As a result, reactions employing the acid-modified catalysts showed considerable reactivity enhancement in RCM. © 2009 Elsevier Ltd. All rights reserved.*
dc.languageEnglish*
dc.titleAcid-mediated activation of modified ring-closing metathesis catalysts*
dc.typeArticle*
dc.relation.issue4*
dc.relation.volume51*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage709*
dc.relation.lastpage713*
dc.relation.journaltitleTetrahedron Letters*
dc.identifier.doi10.1016/j.tetlet.2009.11.112*
dc.identifier.wosidWOS:000274885600038*
dc.identifier.scopusid2-s2.0-72149090380*
dc.author.googleKim S.*
dc.author.googleHwang W.*
dc.author.googleLim I.S.*
dc.author.googleKim S.H.*
dc.author.googleLee S.-g.*
dc.author.googleKim B.M.*
dc.contributor.scopusid이상기(15082786300)*
dc.date.modifydate20240123104103*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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