Issue 0, 1968

Cyto-active amino-acids and peptides. Part XV. The synthesis of p-di-(2-chloroethyl)aminophenyl-L-alanine (melphalan) labelled with tritium

Abstract

Experiments aimed at the preparation of ring-tritiated melphalan by the catalytic replacement of iodine are described. Owing to the lability of tritium ortho to the amino ring-substituent much of the incorporated radioactivity was subsequently lost. Nevertheless products of high specific activity were obtained, suitable for most metabolic and mechanism of action studies.

Article information

Article type
Paper

J. Chem. Soc. C, 1968, 2564-2567

Cyto-active amino-acids and peptides. Part XV. The synthesis of p-di-(2-chloroethyl)aminophenyl-L-alanine (melphalan) labelled with tritium

R. Wade and T. S. Murthy, J. Chem. Soc. C, 1968, 2564 DOI: 10.1039/J39680002564

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