(Chemical Equation Presented) No metal required: A protocol for the enantioselective organocatalytic chlorination of cyclic and acyclic β-keto esters and cyclic β-diketones has been developed which is also effective for the asymmetric bromination of β-keto esters. The methodology employs an inexpensive organocatalyst (e.g. benzoylquinidine) and polyhalogenated quinolinones as the source of the halogen (see scheme). © 2005 Wiley-VCH Verlag GmbH & Co. KGaA.

Organocatalytic asymmetric α-halogenation of 1,3-dicarbonyl compounds

Carlone, Armando;
2005-01-01

Abstract

(Chemical Equation Presented) No metal required: A protocol for the enantioselective organocatalytic chlorination of cyclic and acyclic β-keto esters and cyclic β-diketones has been developed which is also effective for the asymmetric bromination of β-keto esters. The methodology employs an inexpensive organocatalyst (e.g. benzoylquinidine) and polyhalogenated quinolinones as the source of the halogen (see scheme). © 2005 Wiley-VCH Verlag GmbH & Co. KGaA.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11697/121159
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