Abstract
N-Benzyloxycarbonyl protected α-substituted and αβ- 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.
| Original language | English |
|---|---|
| Pages (from-to) | 276-282 |
| Number of pages | 7 |
| Journal | Synthesis |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 2004 Feb 2 |
Keywords
- Amino acid
- Aminoalkanesulfonic acid
- Epoxide
- Olefin
- Synthesis
ASJC Scopus subject areas
- Catalysis
- Organic Chemistry
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Xu, J., & Xu, S. (2004). A General Route to the Synthesis of N-Protected 1-Substituted and 1,2-Disubstituted Taurines. Synthesis, (2), 276-282. https://doi.org/10.1055/s-2003-44382