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  Department of Chemistry (화학과) 1. Journal Papers

 

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Cited 12 time in webofscience Cited 13 time in scopus
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dc.contributor.authorKu, HY-
dc.contributor.authorJung, J-
dc.contributor.authorKim, SH-
dc.contributor.authorKim, HY-
dc.contributor.authorAhn, KH-
dc.contributor.authorKim, SG-
dc.date.accessioned2016-04-01T01:54:40Z-
dc.date.available2016-04-01T01:54:40Z-
dc.date.created2009-08-13-
dc.date.issued2006-04-03-
dc.identifier.issn0957-4166-
dc.identifier.other2006-OAK-0000005995-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/23980-
dc.description.abstractA quick route to enantiomerically pure unnatural aryl glycinols and aryl glycines has been established based on an asymmetric azidation reaction using a chiral benzosultam auxiliary. The synthesis of aryl glycinols involves three steps starting from arylacetic acids, and the chiral auxiliary can be readily recovered. (c) 2006 Elsevier Ltd. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.relation.isPartOfTETRAHEDRON-ASYMMETRY-
dc.subjectALPHA-AMINO-ACIDS-
dc.subjectMETABOTROPIC GLUTAMATE RECEPTORS-
dc.subjectCHIRAL MOLECULAR RECOGNITION-
dc.subjectASYMMETRIC-SYNTHESIS-
dc.subjectPHENYLGLYCINE DERIVATIVES-
dc.subjectARTIFICIAL RECEPTORS-
dc.subjectORGANOAMMONIUM IONS-
dc.subjectARYLGLYCINES-
dc.subjectAUXILIARIES-
dc.subjectENVIRONMENT-
dc.titleAn efficient synthesis of enantiomerically pure unnatural aryl glycinols and aryl glycines-
dc.typeArticle-
dc.contributor.college분자소재융합계의 전자-광 거동연구센터-
dc.identifier.doi10.1016/j.tetasy.2006.03.031-
dc.author.googleKu, HY-
dc.author.googleJung, J-
dc.author.googleKim, SH-
dc.author.googleKim, HY-
dc.author.googleAhn, KH-
dc.author.googleKim, SG-
dc.relation.volume17-
dc.relation.issue7-
dc.relation.startpage1111-
dc.relation.lastpage1115-
dc.contributor.id10087916-
dc.relation.journalTETRAHEDRON-ASYMMETRY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationTETRAHEDRON-ASYMMETRY, v.17, no.7, pp.1111 - 1115-
dc.identifier.wosid000238279900015-
dc.date.tcdate2019-01-01-
dc.citation.endPage1115-
dc.citation.number7-
dc.citation.startPage1111-
dc.citation.titleTETRAHEDRON-ASYMMETRY-
dc.citation.volume17-
dc.contributor.affiliatedAuthorAhn, KH-
dc.identifier.scopusid2-s2.0-33646526018-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc10-
dc.type.docTypeArticle-
dc.subject.keywordPlusMETABOTROPIC GLUTAMATE RECEPTORS-
dc.subject.keywordPlusASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlusPHENYLGLYCINE DERIVATIVES-
dc.subject.keywordPlusMOLECULAR RECOGNITION-
dc.subject.keywordPlusARTIFICIAL RECEPTORS-
dc.subject.keywordPlusAUXILIARIES-
dc.subject.keywordPlusANTAGONISTS-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusAZIDATION-
dc.subject.keywordPlusIONS-
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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안교한AHN, KYO HAN
Dept of Chemistry
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