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dc.contributor.authorShin, Jeong Ah-
dc.contributor.authorChoi, Kyung Il-
dc.contributor.authorPae, Ae Nim-
dc.contributor.authorKoh, Hun Yeong-
dc.contributor.authorKang, H.-Y.-
dc.contributor.authorCho, Yong Seo-
dc.date.accessioned2024-01-21T12:01:34Z-
dc.date.available2024-01-21T12:01:34Z-
dc.date.created2021-09-02-
dc.date.issued2001-09-
dc.identifier.issn1472-7781-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/140230-
dc.description.abstractIndium-mediated allylation of α-chlorocarbonyl compounds with various allyl bromides in aqueous media gave the corresponding homoallylic chlorohydrins, which could be transformed into the corresponding epoxides in the presence of a base. These reactions were strongly dependent upon both the substituents at the carbon bearing chlorine and the allyl bromides used.-
dc.languageEnglish-
dc.titleIndium-mediated allylation reactions of α-chlorocarbonyl compounds and preparation of allylic epoxides-
dc.typeArticle-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJournal of the Chemical Society. Perkin Transactions 1, no.9, pp.946 - 948-
dc.citation.titleJournal of the Chemical Society. Perkin Transactions 1-
dc.citation.number9-
dc.citation.startPage946-
dc.citation.endPage948-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.identifier.scopusid2-s2.0-0035821576-
dc.type.docTypeArticle-
dc.subject.keywordPlusChromatography-
dc.subject.keywordPlusDehalogenation-
dc.subject.keywordPlusExtraction-
dc.subject.keywordPlusMixtures-
dc.subject.keywordPlusNuclear magnetic resonance spectroscopy-
dc.subject.keywordPlusQuenching-
dc.subject.keywordPlusSilica gel-
dc.subject.keywordPlusSolutions-
dc.subject.keywordPlusSubstrates-
dc.subject.keywordPlusSynthesis (chemical)-
dc.subject.keywordPlusAllylation reactions-
dc.subject.keywordPlusSilica gel chromatography-
dc.subject.keywordPlusAromatic hydrocarbons-
dc.subject.keywordAuthorindium-mediated allylation-
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