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Cited 17 time in webofscience Cited 17 time in scopus
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dc.contributor.authorKim, HC-
dc.contributor.authorChoi, S-
dc.contributor.authorKim, H-
dc.contributor.authorAhn, KH-
dc.contributor.authorKoh, JH-
dc.contributor.authorPark, J-
dc.date.accessioned2016-03-31T14:11:14Z-
dc.date.available2016-03-31T14:11:14Z-
dc.date.created2009-03-16-
dc.date.issued1997-06-02-
dc.identifier.issn0040-4039-
dc.identifier.other1997-OAK-0000009787-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/21301-
dc.description.abstractThe enantiomeric purities of secondary alcohols can be easily analyzed by GC and HPLC through derivatization to the esters of 2,2-disubstituted cyclopropanecarboxylic acids 1, and by H-1 NMR analysis of the esters of 2,2-diphenylcyclopropanecarboxylic acid (Ib). In addition racemic 1,1'-bi-2-naphthol is easily resolved through derivatization to monoesters of 2,2-dimethy]cyclopropanecarboxylic acid (1a), which are crystallized selectively and sequentially in high yields with high optical purities. (C) 1997 Elsevier Science Ltd.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.relation.isPartOfTETRAHEDRON LETTERS-
dc.subjectCHEMICAL-SHIFTS-
dc.subjectEFFICIENT-
dc.subjectREAGENTS-
dc.subjectH-1-NMR-
dc.titleChiral 2,2-disubstituted cyclopropanecarboxylic acids: Effective derivatizing agents for analysis of enantiomeric purity of alcohols and for resolution of 1,1'-bi-2-naphthol-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1016/S0040-4039(97)00789-2-
dc.author.googleKim, HC-
dc.author.googleChoi, S-
dc.author.googleKim, H-
dc.author.googleAhn, KH-
dc.author.googleKoh, JH-
dc.author.googlePark, J-
dc.relation.volume38-
dc.relation.issue22-
dc.relation.startpage3959-
dc.relation.lastpage3962-
dc.contributor.id10075891-
dc.relation.journalTETRAHEDRON LETTERS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.38, no.22, pp.3959 - 3962-
dc.identifier.wosidA1997XC48000045-
dc.date.tcdate2019-01-01-
dc.citation.endPage3962-
dc.citation.number22-
dc.citation.startPage3959-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume38-
dc.contributor.affiliatedAuthorPark, J-
dc.identifier.scopusid2-s2.0-0031005106-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc17-
dc.type.docTypeArticle-
dc.subject.keywordPlusCHEMICAL-SHIFTS-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusREAGENTS-
dc.subject.keywordPlusH-1-NMR-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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박재욱PARK, JAIWOOK
Dept of Chemistry
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