Issue 3, 1987

Nucleophilic ring opening of aziridine-2-carboxylates with Wittig reagents; an enantioefficient synthesis of unsaturated amino acids

Abstract

Reaction of N-tosyl- or N-acyl aziridine-(2S)-carboxylate esters with carbonyl stabilized Wittig reagents provides an isolable phosphorus ylide resulting from opening of the aziridine ring; this ylide reacts with carbonyl compounds to provide a novel synthesis of optically pure unsaturated amino acids, exemplified by enantioefficient syntheses of the naturally occuring (2S)-γ-methyleneglutamic acid and (E)-(2S)-4-ethylideneglutamic acid.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 153-155

Nucleophilic ring opening of aziridine-2-carboxylates with Wittig reagents; an enantioefficient synthesis of unsaturated amino acids

J. E. Baldwin, R. M. Adlington and N. G. Robinson, J. Chem. Soc., Chem. Commun., 1987, 153 DOI: 10.1039/C39870000153

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