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Stereoselective Synthesis of Diverse alpha-Hydroxy-beta-amino Acids and It's Application for Synthesis of Dipeptide Expecting as a Protease Inhibitor

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dc.contributor.authorJang, Sang Hun-
dc.contributor.authorKim, Ju Young-
dc.contributor.authorKim, Min Kyu-
dc.contributor.authorHan, Jeong Woo-
dc.contributor.authorPark, Ki Hun-
dc.contributor.authorYoon, Yong-Jin-
dc.contributor.authorLee, Sang-Gyeong-
dc.date.accessioned2022-12-27T05:20:47Z-
dc.date.available2022-12-27T05:20:47Z-
dc.date.issued2009-01-20-
dc.identifier.issn0253-2964-
dc.identifier.issn1229-5949-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/26419-
dc.description.abstractFew alpha-hydroxy-beta-amino acids were synthesized via various nucleophilic addition of the epoxide and followed by stereoselective nucleophilic substitution reaction and eliminative cleavage of the acetal selectively in diacetal compound. One of the synthesized alpha-hydroxy-beta-amino acid reacted with L-leucine methylester to give corresponding dipeptide in good yields.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleStereoselective Synthesis of Diverse alpha-Hydroxy-beta-amino Acids and It's Application for Synthesis of Dipeptide Expecting as a Protease Inhibitor-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.scopusid2-s2.0-60149092319-
dc.identifier.wosid000263863300030-
dc.identifier.bibliographicCitationBULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.30, no.1, pp 163 - 171-
dc.citation.titleBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.citation.volume30-
dc.citation.number1-
dc.citation.startPage163-
dc.citation.endPage171-
dc.type.docTypeArticle-
dc.identifier.kciidART001524143-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusRENIN INHIBITOR-
dc.subject.keywordPlusENANTIOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusKEY COMPONENTS-
dc.subject.keywordPlusESTER UNITS-
dc.subject.keywordPlusSIDE-CHAIN-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusDIHYDROXYLATION-
dc.subject.keywordPlusOLEFINS-
dc.subject.keywordAuthoralpha-Hydroxy-beta-amino acids-
dc.subject.keywordAuthorNucleophilic addition-
dc.subject.keywordAuthorEpoxide ring opening-
dc.subject.keywordAuthorEliminative cleavage-
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