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dc.contributor.author김관묵-
dc.date.accessioned2017-08-28T20:04:25Z-
dc.date.available2017-08-28T20:04:25Z-
dc.date.issued2009-
dc.identifier.issn0040-4020-
dc.identifier.otherOAK-5353-
dc.identifier.urihttp://dspace.ewha.ac.kr/handle/2015.oak/231881-
dc.description.abstractNovel binol receptor with pyrrole-2-carboxamide moiety and its analogues have been designed, synthesized, and used to enantioselectively recognize 1,2-aminoalcohols via multiple hydrogen bonding. The pyrrole-based binol receptor showed the highest enantioselectivity among the four receptors as determined by the 1H NMR. The DFT calculation strongly supports complementary hydrogen bonding between alcoholic -OH and pyrrolyl groups. © 2008 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.titleEnantioselective recognition of 1,2-aminoalcohols by the binol receptor dangled with pyrrole-2-carboxamide and its analogues-
dc.typeArticle-
dc.relation.issue3-
dc.relation.volume65-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage666-
dc.relation.lastpage671-
dc.relation.journaltitleTetrahedron-
dc.identifier.doi10.1016/j.tet.2008.11.022-
dc.identifier.wosidWOS:000262773800010-
dc.identifier.scopusid2-s2.0-57149122415-
dc.author.googleNandhakumar R.-
dc.author.googleSoo A.Y.-
dc.author.googleHong J.-
dc.author.googleHam S.-
dc.author.googleKim K.M.-
dc.contributor.scopusid김관묵(35484385500)-
dc.date.modifydate20170601140242-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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