Abstract
A series of 1-substituted taurines, including optically active taurines, were synthesized
expeditiously from epoxides via episulfidation with potassium sulfocyanate, ring-opening
with dibenzylamine, followed by oxidation with performic acid, and hydrogenolysis
in the presence of palladium hydroxide on carbon powder. This method was also used
for the synthesis of trans -cyclic taurines.
Key words
amino acid - aminoalkanesulfonic acid - epoxide - episulfide - synthesis - taurine
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