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Synthesis 2004(2): 276-282
DOI: 10.1055/s-2003-44382
DOI: 10.1055/s-2003-44382
PAPER
© Georg Thieme Verlag Stuttgart · New York
A General Route to the Synthesis of N-Protected 1-Substituted and 1,2-Disubstituted Taurines
Weitere Informationen
Received
8 October 2003
Publikationsdatum:
15. Dezember 2003 (online)
Publikationsverlauf
Publikationsdatum:
15. Dezember 2003 (online)
![](https://www.thieme-connect.de/media/synthesis/200402/lookinside/thumbnails/10.1055-s-2003-44382-1.jpg)
Abstract
N-Benzyloxycarbonyl protected α-substituted and α,β-disubstituted taurines were synthesized from olefins and epoxides via N-benzyloxycarbonylamino alcohol thioacetates as key intermediates. They are important sulfur analogues of naturally occurring amino acids and building blocks for the synthesis of α-substituted and α,β-disubstituted β-sulfonopeptides.
Key words
amino acid - aminoalkanesulfonic acid - epoxide - olefin - synthesis
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