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Cited 21 time in webofscience Cited 22 time in scopus
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dc.contributor.authorYu, SH-
dc.contributor.authorChung, SK-
dc.date.accessioned2016-03-31T12:35:22Z-
dc.date.available2016-03-31T12:35:22Z-
dc.date.created2009-02-28-
dc.date.issued2004-02-23-
dc.identifier.issn0957-4166-
dc.identifier.other2004-OAK-0000004058-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/18068-
dc.description.abstractD and L forms of carba-beta-altrose 8, carba-beta-mannose 10a, carba-beta-idose 12, carba-beta-talose 14 derivatives were prepared from (+/-)-3-cyclohexene-1-carboxylic acid 1. Homochiral diol compounds D-5a and L-5a, which were prepared from 1 via enzyme resolution of (+/-)-4a, were efficiently transformed to carba-beta-altrose derivatives 8 by stereoselective introduction of hydroxyl groups. Oxidation (PCC)/reduction (NaBH4) of 3-OH and/or 4-OH of 8a efficiently gave 10a, 12, and 14 with good stereoselectivity. (C) 2004 Elsevier Ltd. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.relation.isPartOfTETRAHEDRON-ASYMMETRY-
dc.subjectPSEUDO-SUGARS-
dc.subjectALPHA-D-
dc.subjectALLYLIC ALCOHOLS-
dc.subjectHEPARIN-
dc.subjectPOLYSACCHARIDE-
dc.subjectPENTAACETATES-
dc.subjectEPOXIDES-
dc.subjectFK-506-
dc.subjectACID-
dc.titlePractical syntheses of enantiopure carbasugars: carba-beta-altrose, carba-beta-mannose, carba-beta-idose, and carba-beta-talose derivatives-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1016/j.tetasy.2003.12.042-
dc.author.googleYu, SH-
dc.author.googleChung, SK-
dc.relation.volume15-
dc.relation.issue4-
dc.relation.startpage581-
dc.relation.lastpage584-
dc.contributor.id10200284-
dc.relation.journalTETRAHEDRON-ASYMMETRY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationTETRAHEDRON-ASYMMETRY, v.15, no.4, pp.581 - 584-
dc.identifier.wosid000189116300003-
dc.date.tcdate2019-01-01-
dc.citation.endPage584-
dc.citation.number4-
dc.citation.startPage581-
dc.citation.titleTETRAHEDRON-ASYMMETRY-
dc.citation.volume15-
dc.contributor.affiliatedAuthorChung, SK-
dc.identifier.scopusid2-s2.0-1042298828-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc19-
dc.type.docTypeArticle-
dc.subject.keywordPlusPSEUDO-SUGARS-
dc.subject.keywordPlusALPHA-D-
dc.subject.keywordPlusALLYLIC ALCOHOLS-
dc.subject.keywordPlusHEPARIN-
dc.subject.keywordPlusPOLYSACCHARIDE-
dc.subject.keywordPlusPENTAACETATES-
dc.subject.keywordPlusEPOXIDES-
dc.subject.keywordPlusFK-506-
dc.subject.keywordPlusACID-
dc.relation.journalWebOfScienceCategoryChemistry, Inorganic & Nuclear-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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