DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, HC | - |
dc.contributor.author | Choi, S | - |
dc.contributor.author | Kim, H | - |
dc.contributor.author | Ahn, KH | - |
dc.contributor.author | Koh, JH | - |
dc.contributor.author | Park, J | - |
dc.date.accessioned | 2016-03-31T14:11:14Z | - |
dc.date.available | 2016-03-31T14:11:14Z | - |
dc.date.created | 2009-03-16 | - |
dc.date.issued | 1997-06-02 | - |
dc.identifier.issn | 0040-4039 | - |
dc.identifier.other | 1997-OAK-0000009787 | - |
dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/21301 | - |
dc.description.abstract | The 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.statementofresponsibility | X | - |
dc.language | English | - |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
dc.relation.isPartOf | TETRAHEDRON LETTERS | - |
dc.subject | CHEMICAL-SHIFTS | - |
dc.subject | EFFICIENT | - |
dc.subject | REAGENTS | - |
dc.subject | H-1-NMR | - |
dc.title | Chiral 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.type | Article | - |
dc.contributor.college | 화학과 | - |
dc.identifier.doi | 10.1016/S0040-4039(97)00789-2 | - |
dc.author.google | Kim, HC | - |
dc.author.google | Choi, S | - |
dc.author.google | Kim, H | - |
dc.author.google | Ahn, KH | - |
dc.author.google | Koh, JH | - |
dc.author.google | Park, J | - |
dc.relation.volume | 38 | - |
dc.relation.issue | 22 | - |
dc.relation.startpage | 3959 | - |
dc.relation.lastpage | 3962 | - |
dc.contributor.id | 10075891 | - |
dc.relation.journal | TETRAHEDRON LETTERS | - |
dc.relation.index | SCI급, SCOPUS 등재논문 | - |
dc.relation.sci | SCI | - |
dc.collections.name | Journal Papers | - |
dc.type.rims | ART | - |
dc.identifier.bibliographicCitation | TETRAHEDRON LETTERS, v.38, no.22, pp.3959 - 3962 | - |
dc.identifier.wosid | A1997XC48000045 | - |
dc.date.tcdate | 2019-01-01 | - |
dc.citation.endPage | 3962 | - |
dc.citation.number | 22 | - |
dc.citation.startPage | 3959 | - |
dc.citation.title | TETRAHEDRON LETTERS | - |
dc.citation.volume | 38 | - |
dc.contributor.affiliatedAuthor | Park, J | - |
dc.identifier.scopusid | 2-s2.0-0031005106 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.wostc | 17 | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | CHEMICAL-SHIFTS | - |
dc.subject.keywordPlus | EFFICIENT | - |
dc.subject.keywordPlus | REAGENTS | - |
dc.subject.keywordPlus | H-1-NMR | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
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