DSpace at KISTKIST Article2003

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dc.contributor.authorAhn, DR-
dc.contributor.authorMosimann, M-
dc.contributor.authorLeumann, CJ-
dc.date.accessioned2024-01-21T08:34:53Z-
dc.date.available2024-01-21T08:34:53Z-
dc.date.created2021-09-01-
dc.date.issued2003-08-
dc.identifier.issn1525-7770-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/138391-
dc.description.abstractcpa-DNA monomers containing the bases adenine and thymine have been synthesized starting from the known compound 1 in 12 steps. Partially and fully modified cpa-thymidine and cpa-adenosine containing oligodcoxynucleotides were synthesized by standard oligonucleotide chemistry. Fully modified homo-cpa-A sequences lead to duplex destabilization by -1.4degreesC/mod. relative to DNA. As its congener bca-DNA, cpa-DNA prefers left-handed duplex formation where possible.-
dc.languageEnglish-
dc.publisherMARCEL DEKKER INC-
dc.titleSynthesis of a cyclopentane amide DNA analogue and its base pairing properties-
dc.typeArticle-
dc.identifier.doi10.1081/NCN-120022837-
dc.description.journalClass1-
dc.identifier.bibliographicCitationNUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, v.22, no.5-8, pp.1207 - 1210-
dc.citation.titleNUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS-
dc.citation.volume22-
dc.citation.number5-8-
dc.citation.startPage1207-
dc.citation.endPage1210-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000185439200157-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.type.docTypeArticle; Proceedings Paper-
dc.subject.keywordAuthorcpa-
dc.subject.keywordAuthorbicyclic DNA-
dc.subject.keywordAuthorcyclopentane-
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