Please use this identifier to cite or link to this item:
|Title:||Enantioselective organocatalytic fluorination using organofluoro nucleophiles|
|Authors:||Zhao, Y. |
|Citation:||Zhao, 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|
|Abstract:||Synthetic 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.|
|Source Title:||Organic and Biomolecular Chemistry|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Jul 17, 2018
WEB OF SCIENCETM
checked on Jun 27, 2018
checked on Jun 15, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.