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Synthesis 2005(13): 2122-2128
DOI: 10.1055/s-2005-869994
DOI: 10.1055/s-2005-869994
PAPER
© Georg Thieme Verlag Stuttgart · New York
An Expeditious Synthesis of 1-Substituted and Cyclic Taurines
Further Information
Received
20 January 2005
Publication Date:
13 July 2005 (online)
Publication History
Publication Date:
13 July 2005 (online)
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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