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. 1977 Aug 15;33(8):1118-9.
doi: 10.1007/BF01946005.

A facile one-step synthesis of cysteinyldopas using mushroom tyrosinase

A facile one-step synthesis of cysteinyldopas using mushroom tyrosinase

S Ito et al. Experientia. .

Abstract

A convenient one-step procedure, based upon the tyrosinase co-oxidation of dopa and cysteine, is reported for the synthesis of 5-S-cysteinyldopa (I) in 74% yield. Secondary products of the reaction turned out to be 2-S-cysteinyldopa (II, 14%), 2,5-S, S-dicysteinyldopa (iv, 5%), and the hitherto unknown 6-S-cysteinyldopa (III, approximately 1%).

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