DSpace at KISTKIST Article2002

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dc.contributor.authorMoon, HR-
dc.contributor.authorKim, HO-
dc.contributor.authorLee, KM-
dc.contributor.authorChun, MW-
dc.contributor.authorKim, JH-
dc.contributor.authorJeong, LS-
dc.date.accessioned2024-01-21T10:01:30Z-
dc.date.available2024-01-21T10:01:30Z-
dc.date.created2021-09-01-
dc.date.issued2002-10-03-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/139137-
dc.description.abstract[GRAPHICS] A total synthesis of apio-neplanocin A, which combines properties of apio nucleoside and neplanocin A and is a potential inhibitor of S-adenosylhomocysteine hydrolase, was accomplished starting from D-ribose via stereoselective hydroxymethylation and RCM reaction.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectCARBOCYCLIC ADENOSINE-ANALOGS-
dc.subject2&apos-
dc.subject-DEOXY-3&apos-
dc.subject-THIACYTIDINE BCH-189-
dc.subjectANTIVIRAL ACTIVITY-
dc.subjectL929 CELLS-
dc.subjectMECHANISM-
dc.subjectSPECTRUM-
dc.subjectINVITRO-
dc.subjectTARGET-
dc.subjectAGENTS-
dc.titleStereoselective synthesis of a novel apio analogue of neplanocin A as potential S-adenosylhomocysteine hydrolase inhibitor-
dc.typeArticle-
dc.identifier.doi10.1021/ol026624m-
dc.description.journalClass1-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.4, no.20, pp.3501 - 3503-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume4-
dc.citation.number20-
dc.citation.startPage3501-
dc.citation.endPage3503-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000178327500042-
dc.identifier.scopusid2-s2.0-0037015428-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusCARBOCYCLIC ADENOSINE-ANALOGS-
dc.subject.keywordPlus2&apos-
dc.subject.keywordPlus-DEOXY-3&apos-
dc.subject.keywordPlus-THIACYTIDINE BCH-189-
dc.subject.keywordPlusANTIVIRAL ACTIVITY-
dc.subject.keywordPlusL929 CELLS-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusSPECTRUM-
dc.subject.keywordPlusINVITRO-
dc.subject.keywordPlusTARGET-
dc.subject.keywordPlusAGENTS-
dc.subject.keywordAuthorsynthesis-
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