(Boc-Cys-OH)₂
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Product Description
Tai et al. could obtain asymmetric cystine peptides from (Boc-Cys-OH)₂ by enzymatic catalysis with immobilized papain. Oxidation of Boc-cystine with hydrogen peroxide in the presence of Na wolframate yielded the sodium salt of Boc-cysteic acid. Boc cystine benzyl ester was used as educt for obtaining S-isoacyl dipeptide building blocks.