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Article Dans Une Revue Chemistry - A European Journal Année : 2012

Preparation of Chiral Amino Esters by Asymmetric Phase-Transfer Catalyzed Alkylations of Schiff Bases in a Ball Mill

Résumé

The asymmetric alkylation of Schiff bases under basic conditions in a ball mill was performed. The starting Schiff bases of glycine were prepared beforehand by milling protected glycine hydrochloride and benzophenone imine, in the absence of solvent. The Schiff base was then reacted with a halogenated derivative in a ball mill in the presence of KOH. By adding a chiral ammonium salt derived from cinchonidine, the reaction proceeded asymmetrically under phase-transfer catalysis conditions, giving excellent yields and enantiomeric excesses up to 75%. Because an equimolar amount of starting material was used, purification was greatly simplified.
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Dates et versions

hal-00680294 , version 1 (12-02-2021)

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Citer

Pierrick Nun, Violaine Pérez, Monique Calmes, Jean Martinez, Frédéric Lamaty. Preparation of Chiral Amino Esters by Asymmetric Phase-Transfer Catalyzed Alkylations of Schiff Bases in a Ball Mill. Chemistry - A European Journal, 2012, 18, pp.3773-3779. ⟨10.1002/chem.201102885⟩. ⟨hal-00680294⟩
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