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dc.contributor.authorSong, CE-
dc.contributor.authorOh, CR-
dc.contributor.authorLee, SW-
dc.contributor.authorLee, SG-
dc.contributor.authorCanali, L-
dc.contributor.authorSherrington, DC-
dc.date.accessioned2024-01-21T16:32:12Z-
dc.date.available2024-01-21T16:32:12Z-
dc.date.created2021-09-03-
dc.date.issued1998-11-21-
dc.identifier.issn1359-7345-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/142724-
dc.description.abstractExcellent enantioselectivities of up to > 99% ee have been achieved in the heterogeneous asymmetric aminohydroxylation of trans-cinnamate derivatives using silica gel-supported (QN)(2)PHAL [SGS-(QN)(2)PHAL 1]; the dark brown 1.0s complex, recovered by simple filtration after reaction, could be reused without any loss of enantioselectivity.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectOLEFINS-
dc.subjectDIHYDROXYLATION-
dc.subjectEFFICIENT-
dc.titleHeterogeneous asymmetric aminohydroxylation of alkenes using a silica gel-supported bis-cinchona alkaloid-
dc.typeArticle-
dc.identifier.doi10.1039/a806959j-
dc.description.journalClass1-
dc.identifier.bibliographicCitationCHEMICAL COMMUNICATIONS, no.22, pp.2435 - 2436-
dc.citation.titleCHEMICAL COMMUNICATIONS-
dc.citation.number22-
dc.citation.startPage2435-
dc.citation.endPage2436-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000077083700007-
dc.identifier.scopusid2-s2.0-0032556374-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusOLEFINS-
dc.subject.keywordPlusDIHYDROXYLATION-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordAuthorheterogeneous asymmetric aminohydroxylation-
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