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dc.contributor.authorKim, DC-
dc.contributor.authorYoo, KH-
dc.contributor.authorKim, DJ-
dc.contributor.authorChung, BY-
dc.contributor.authorPark, SW-
dc.date.accessioned2024-01-21T15:15:58Z-
dc.date.available2024-01-21T15:15:58Z-
dc.date.created2022-01-11-
dc.date.issued1999-06-25-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/142113-
dc.description.abstractNovel N-acetyl C-aza-2-deoxy-D-ribonucleosides were synthesized from 2-deoxy-D-ribose via a consecutive procedure of the addition of ortho-lithiated pyrimidine salt, Staudinger-aza-Wittig ring cyclization, and reduction of cyclic imine. (C) 1999 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectOLIGONUCLEOTIDES-
dc.subjectANALOG-
dc.subjectHETEROCYCLES-
dc.subjectINHIBITORS-
dc.subjectNITROGEN-
dc.titleSynthesis of new pyrrolidine C-nucleosides via Staudinger-aza-Wittig cyclization of gamma-azido ketone-
dc.typeArticle-
dc.identifier.doi10.1016/S0040-4039(99)00854-0-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.40, no.26, pp.4825 - 4828-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume40-
dc.citation.number26-
dc.citation.startPage4825-
dc.citation.endPage4828-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000081122200020-
dc.identifier.scopusid2-s2.0-0033603434-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusOLIGONUCLEOTIDES-
dc.subject.keywordPlusANALOG-
dc.subject.keywordPlusHETEROCYCLES-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusNITROGEN-
dc.subject.keywordAuthorpyrrolidine C-nucleosides-
dc.subject.keywordAuthorStaudinger-aza-Wittig cyclization-
dc.subject.keywordAuthorgamma-azido ketone-
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