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Enantioselective halogenation via asymmetric phase-transfer catalysis
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dc.contributor.author Lee, Sunggi -
dc.contributor.author Chung, Won-jin -
dc.date.accessioned 2022-11-02T07:00:24Z -
dc.date.available 2022-11-02T07:00:24Z -
dc.date.created 2022-06-16 -
dc.date.issued 2022-07 -
dc.identifier.issn 0253-2964 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/17029 -
dc.description.abstract The asymmetric phase-transfer catalysis (PTC) is a flourishing field of contemporary synthetic organic chemistry, and this prominent methodology has been tremendously successful in enantioselective halogenations. Both electrophilic and nucleophilic reaction manifolds were enabled through the exploitation of highly ordered ion pairing and/or hydrogen-bonding interactions around a carefully designed chiral phase-transfer catalyst with an insoluble halogenating reagent as well as a suitable substrate. Fluorination has been the most fruitful, and encouraging results have also been documented with heavier halogens. This review surveys examples of various enantioselective halogenations via the asymmetric PTC from its beginning to prosperity over the past decade. © 2022 Korean Chemical Society, Seoul & Wiley-VCH GmbH. -
dc.language English -
dc.publisher 대한화학회 -
dc.title Enantioselective halogenation via asymmetric phase-transfer catalysis -
dc.type Article -
dc.identifier.doi 10.1002/bkcs.12546 -
dc.identifier.wosid 000804691400001 -
dc.identifier.scopusid 2-s2.0-85131190020 -
dc.identifier.bibliographicCitation Lee, Sunggi. (2022-07). Enantioselective halogenation via asymmetric phase-transfer catalysis. Bulletin of the Korean Chemical Society, 43(7), 896–911. doi: 10.1002/bkcs.12546 -
dc.identifier.kciid ART002861209 -
dc.description.isOpenAccess FALSE -
dc.subject.keywordAuthor enantioselectivity -
dc.subject.keywordAuthor halogenation -
dc.subject.keywordAuthor hydrogen bonding -
dc.subject.keywordAuthor ion pairing -
dc.subject.keywordAuthor phase-transfer catalysis -
dc.subject.keywordPlus BETA-KETO-ESTERS -
dc.subject.keywordPlus QUATERNARY PHOSPHONIUM SALTS -
dc.subject.keywordPlus SUPPORTED IONIC LIQUIDS -
dc.subject.keywordPlus CHIRAL ANION -
dc.subject.keywordPlus CINCHONA ALKALOIDS -
dc.subject.keywordPlus ALLYLIC ALCOHOLS -
dc.subject.keywordPlus HYDROGEN-BOND -
dc.subject.keywordPlus FLUORINATIVE DEAROMATIZATION -
dc.subject.keywordPlus NUCLEOPHILIC FLUORINATION -
dc.subject.keywordPlus EFFICIENT SYNTHESIS -
dc.citation.endPage 911 -
dc.citation.number 7 -
dc.citation.startPage 896 -
dc.citation.title Bulletin of the Korean Chemical Society -
dc.citation.volume 43 -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.description.journalRegisteredClass kci -
dc.relation.journalResearchArea Chemistry -
dc.relation.journalWebOfScienceCategory Chemistry, Multidisciplinary -
dc.type.docType Review -
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