Please use this identifier to cite or link to this item: https://doi.org/10.1039/c1ob05840a
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dc.titleEnantioselective organocatalytic fluorination using organofluoro nucleophiles
dc.contributor.authorZhao, Y.
dc.contributor.authorPan, Y.
dc.contributor.authorSim, S.-B.D.
dc.contributor.authorTan, C.-H.
dc.date.accessioned2014-06-23T05:57:06Z
dc.date.available2014-06-23T05:57:06Z
dc.date.issued2012-01-21
dc.identifier.citationZhao, Y., Pan, Y., Sim, S.-B.D., Tan, C.-H. (2012-01-21). Enantioselective organocatalytic fluorination using organofluoro nucleophiles. Organic and Biomolecular Chemistry 10 (3) : 479-485. ScholarBank@NUS Repository. https://doi.org/10.1039/c1ob05840a
dc.identifier.issn14770520
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/77601
dc.description.abstractSynthetic fluorinated compounds are enormously useful in areas such as materials, agrochemicals, pharmaceuticals and fine chemicals. While methods of electrophilic fluorination have been extensively developed to stereoselectively install fluorine atoms onto molecules, nucleophilic fluorination is a much less explored approach. Recently, several organofluoro reagents have been designed and used as nucleophiles in the asymmetric synthesis of fluorinated compounds, significantly expanding the scope of enantio-enriched fluorine-containing compounds that can be synthesised. Such organofluoro nucleophiles are particularly useful in organocatalytic transformations. In this review, recent advances in the application of organofluoro nucleophiles in organocatalysis are summarised.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c1ob05840a
dc.sourceScopus
dc.typeReview
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c1ob05840a
dc.description.sourcetitleOrganic and Biomolecular Chemistry
dc.description.volume10
dc.description.issue3
dc.description.page479-485
dc.identifier.isiut000298750800001
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