Issue 10, 1993

Synthesis of unsaturated α-amino acids using the Ramberg–Bäcklund reaction

Abstract

A novel, and potentially versatile, procedure for the preparation of unsaturated α-amino acids in homochiral form is illustrated by the conversion of methionine into allylglycine (as its Boc, tert-butyl ester derivative) using the Ramberg–Bäcklund reaction in the key step.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 874-875

Synthesis of unsaturated α-amino acids using the Ramberg–Bäcklund reaction

Z. Guo, M. J. Schaeffer and R. J. K. Taylor, J. Chem. Soc., Chem. Commun., 1993, 874 DOI: 10.1039/C39930000874

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