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synthesis of chiral 2,3-diamino acid derivatives using diaza-cope rearrangement

DC Field Value Language
dc.contributor.advisor김병문-
dc.contributor.author이상민-
dc.date.accessioned2019-06-25T17:00:40Z-
dc.date.available2019-06-25T17:00:40Z-
dc.date.issued2012-02-
dc.identifier.other000000000511-
dc.identifier.urihttps://hdl.handle.net/10371/155915-
dc.identifier.urihttp://dcollection.snu.ac.kr/jsp/common/DcLoOrgPer.jsp?sItemId=000000000511-
dc.description학위논문 (석사)-- 서울대학교 대학원 : 화학부, 2012. 2. 김병문.-
dc.description.abstractChiral vicinal diamine derivatives are important starting materials not only for stereoselctive catalysts, but also for diverse durgs. Because of this reasons, many interesting chiral vicinal diamine derivatives have been synthesized by oxidation, reduction, reductive coupling, C-C bond forming reactions and chiral resolutions. We developed a stereospecific synthesis of chiral vicinal α-β-diamino ester Using diaza-Cope rearrangement reaction.-
dc.format.extent42-
dc.language.isoeng-
dc.publisher서울대학교 대학원-
dc.subject.ddc540-
dc.titlesynthesis of chiral 2,3-diamino acid derivatives using diaza-cope rearrangement-
dc.typeThesis-
dc.typeDissertation-
dc.description.degreeMaster-
dc.contributor.affiliation화학부-
dc.date.awarded2012-02-
dc.identifier.holdings000000000006▲000000000011▲000000000511▲-
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