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Beilstein J Org Chem ; 8: 1233-40, 2012.
Article in English | MEDLINE | ID: mdl-23019453

ABSTRACT

A fluorous cinchona alkaloid ester has been developed as a chiral promoter for the asymmetric fluorination of ß-ketoesters. It has comparable reactivity and selectivity to the nonfluorous versions of cinchona alkaloids and can be easily recovered from the reaction mixture by simple fluorous solid-phase extraction (F-SPE) and used for the next round of reaction without further purification.

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