Issue 7, 1996

Spontaneous formation of diastereoisomeric 2-methylthiazolidine-2,4-dicarboxylates from cystine esters and related compounds

Abstract

Dialkyl esters of cystine and lanthionine undergo conversion to cis- and trans-2-methylthiazolidine-2,4-dicarboxylates at 25–80 °C in protic solvents.

Article information

Article type
Paper

Chem. Commun., 1996, 843-844

Spontaneous formation of diastereoisomeric 2-methylthiazolidine-2,4-dicarboxylates from cystine esters and related compounds

R. R. Hill and S. J. Robinson, Chem. Commun., 1996, 843 DOI: 10.1039/CC9960000843

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