Expedient preparation of all isomers of 2-Aminocyclobutanecarboxylic acid in enantiomerically pure form - Archive ouverte HAL
Article Dans Une Revue Journal of Organic Chemistry Année : 2009

Expedient preparation of all isomers of 2-Aminocyclobutanecarboxylic acid in enantiomerically pure form

Résumé

A short, convenient, gram scale protocol has been established to allow facile access to all four stereoisomers of 2-aminocyclobutanecarboxylic acid, each in enantiomerically pure form (ee >99%). Starting from the readily available cis racemate, the procedure combines efficient α-phenylethylamine derivative resolution and controlled cis-to-trans epimerization procedures, and proceeds with invariably high yields
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Dates et versions

hal-00376781 , version 1 (20-04-2009)

Identifiants

  • HAL Id : hal-00376781 , version 1

Citer

Carlos Fernandes, Elisabeth Pereira, Sophie Faure, David J Aitken. Expedient preparation of all isomers of 2-Aminocyclobutanecarboxylic acid in enantiomerically pure form. Journal of Organic Chemistry, 2009, 74, pp.3217-3220. ⟨hal-00376781⟩
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