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Improved stereoselectivity in intramolecular S(N)2 ' cyclization through use of mechanistic principles

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dc.contributor.authorSeo, Woo Duck-
dc.contributor.authorCurtis-Long, Marcus J.-
dc.contributor.authorJeong, Seong Hun-
dc.contributor.authorJun, Tae Hong-
dc.contributor.authorYang, Min Suk-
dc.contributor.authorPark, Ki Hun-
dc.date.accessioned2022-12-27T07:04:15Z-
dc.date.available2022-12-27T07:04:15Z-
dc.date.issued2007-01-17-
dc.identifier.issn0039-7881-
dc.identifier.issn1437-210X-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/28466-
dc.description.abstractValine and alanine were converted into the corresponding alpha-hydroxy-beta-amino acids through intramolecular S(N)2' cyclization. The novel cyclization protocol relied upon the use of N-benzyl-protected carbarnates derived from a-amino acids-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherGEORG THIEME VERLAG KG-
dc.titleImproved stereoselectivity in intramolecular S(N)2 ' cyclization through use of mechanistic principles-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1055/s-2006-958956-
dc.identifier.scopusid2-s2.0-33947493961-
dc.identifier.wosid000243785100005-
dc.identifier.bibliographicCitationSYNTHESIS-STUTTGART, no.2, pp 209 - 214-
dc.citation.titleSYNTHESIS-STUTTGART-
dc.citation.number2-
dc.citation.startPage209-
dc.citation.endPage214-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusBETA-AMINO ACIDS-
dc.subject.keywordPlusENANTIOSELECTIVE SYNTHESIS-
dc.subject.keywordPlus1,3-ALLYLIC STRAIN-
dc.subject.keywordPlusRENIN INHIBITORS-
dc.subject.keywordPlusHETEROCYCLES-
dc.subject.keywordPlusPYRROLIDINES-
dc.subject.keywordPlusALDEHYDES-
dc.subject.keywordPlusSYN-
dc.subject.keywordAuthoroxazolidin-2-one-
dc.subject.keywordAuthorintramolecular cyclization-
dc.subject.keywordAuthorstereoselectivity-
dc.subject.keywordAuthorA(1,3) strain-
dc.subject.keywordAuthoralpha-hydroxy-beta-amino acids-
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