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Enantioselective halogenation via asymmetric phase-transfer catalysis
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Title
Enantioselective halogenation via asymmetric phase-transfer catalysis
Issued Date
2022-07
Citation
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
Type
Article
Author Keywords
enantioselectivityhalogenationhydrogen bondingion pairingphase-transfer catalysis
Keywords
BETA-KETO-ESTERSQUATERNARY PHOSPHONIUM SALTSSUPPORTED IONIC LIQUIDSCHIRAL ANIONCINCHONA ALKALOIDSALLYLIC ALCOHOLSHYDROGEN-BONDFLUORINATIVE DEAROMATIZATIONNUCLEOPHILIC FLUORINATIONEFFICIENT SYNTHESIS
ISSN
0253-2964
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.
URI
http://hdl.handle.net/20.500.11750/17029
DOI
10.1002/bkcs.12546
Publisher
대한화학회
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Department of Physics and Chemistry

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