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dc.contributor.authorLee, JG-
dc.contributor.authorChoi, KI-
dc.contributor.authorPae, AN-
dc.contributor.authorKoh, HY-
dc.contributor.authorKang, YH-
dc.contributor.authorCho, YS-
dc.date.accessioned2024-01-21T10:45:34Z-
dc.date.available2024-01-21T10:45:34Z-
dc.date.created2021-09-05-
dc.date.issued2002-04-
dc.identifier.issn1472-7781-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/139661-
dc.description.abstractThe hemiacetals of (+)- and (-)-N-glyoxyloylbornane-10,2-sultam and their imines reacted with allyl iodide in the presence of indium in DMF to give the corresponding alpha-hydroxy and alpha-amino camphor sultam derivatives with high diastereoselectivities (86-90% de). This method could be useful for preparation of alpha-hydroxy and alpha-amino acids.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleIndium-mediated diastereoselective allylation reactions: preparation of alpha-hydroxy and alpha-amino acids-
dc.typeArticle-
dc.identifier.doi10.1039/b110505c-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, no.10, pp.1314 - 1317-
dc.citation.titleJOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1-
dc.citation.number10-
dc.citation.startPage1314-
dc.citation.endPage1317-
dc.description.journalRegisteredClassscie-
dc.identifier.wosid000175509800016-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordAuthordiastereoselective-
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