Issue 19, 1995

Stereoselective synthesis of α-alkylated γ,δ-unsaturated amino acids via Claisen rearrangement of chelated enolates

Abstract

Ester enolate Claisen rearrangement of chelated N-protected amino acid allylic esters results in the formation of α-alkylated γ,δ-unsaturated amino acids in good yields and in a highly diastereoselective fashion.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 1991-1992

Stereoselective synthesis of α-alkylated γ,δ-unsaturated amino acids via Claisen rearrangement of chelated enolates

U. Kazmaier and S. Maier, J. Chem. Soc., Chem. Commun., 1995, 1991 DOI: 10.1039/C39950001991

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