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dc.contributor.author정낙신-
dc.contributor.author최원준-
dc.date.accessioned2016-11-26T02:11:36Z-
dc.date.available2016-11-26T02:11:36Z-
dc.date.issued2008-
dc.identifier.issn1934-9289-
dc.identifier.otherOAK-17992-
dc.identifier.urihttp://dspace.ewha.ac.kr/handle/2015.oak/232851-
dc.description.abstractFluoroneplanocin A, designed as a potent mechanism-based irreversible inhibitor of S-adenosylhomocysteine hydrolase (SAH), is synthesized from D-ribose via a key D-cyclopentenone intermediate. This intermediate is synthesized using a stereoselective Grignard reaction, a ring-closing metathesis (RCM) reaction, and oxidative rearrangement as key steps.-
dc.languageEnglish-
dc.titleSynthesis of fluoroneplanocin A.-
dc.typeArticle-
dc.relation.volumeChapter 14-
dc.relation.indexSCOPUS-
dc.relation.journaltitleCurrent protocols in nucleic acid chemistry / edited by Serge L. Beaucage ... [et al.]-
dc.identifier.scopusid2-s2.0-55949083780-
dc.author.googleJeong L.S.-
dc.author.googleTosh D.K.-
dc.author.googleChoi W.J.-
dc.author.googlePal S.-
dc.date.modifydate20200911081002-
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약학대학 > 약학과 > Journal papers
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