DSpace at KISTKIST Article2005

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dc.contributor.authorJun, SJ-
dc.contributor.authorMoon, MS-
dc.contributor.authorLee, SH-
dc.contributor.authorCheong, CS-
dc.contributor.authorKim, KS-
dc.date.accessioned2024-01-21T04:38:06Z-
dc.date.available2024-01-21T04:38:06Z-
dc.date.created2021-09-03-
dc.date.issued2005-07-25-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/136281-
dc.description.abstractMethyl arabinofuranoside 1 was fully acetylated to methyl 2,3,5-tri-O-acetyl-D-arabinofuranoside 2 and it was regio-selectively deacetylated using enzymes. Rhizopus oryzae esterase gave methyl 3,5-di-O-acetyl-D-arabinofuranoside 3, regioselectively. This protected 3 was deoxygenized to 3,5-di-O-acetyl-D-2-deoxyarabinofuranoside 7 using hypophosphorous acid. (c) 2005 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectLIPASE-
dc.subjectDEOXYGENATION-
dc.subjectHYDROLYSIS-
dc.subjectANALOGS-
dc.titleSelective monodeacetylation of methyl 2,3,5-tri-O-acetyl-D-arabinofuranoside using biocatalyst-
dc.typeArticle-
dc.identifier.doi10.1016/j.tetlet.2005.05.120-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.46, no.30, pp.5063 - 5065-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume46-
dc.citation.number30-
dc.citation.startPage5063-
dc.citation.endPage5065-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000230362300030-
dc.identifier.scopusid2-s2.0-20544432003-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusLIPASE-
dc.subject.keywordPlusDEOXYGENATION-
dc.subject.keywordPlusHYDROLYSIS-
dc.subject.keywordPlusANALOGS-
dc.subject.keywordAuthorarabinose-
dc.subject.keywordAuthor2-deoxyarabinofuranoside-
dc.subject.keywordAuthorenzyme-
dc.subject.keywordAuthorresolution-
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