Stereoselective synthesis and peptide incorporation of (S)-.alpha.-amino-(2,2'-bipyridine)-6-propanoic acid
โ Scribed by Imperiali, Barbara; Fisher, Stewart L.
- Book ID
- 126294447
- Publisher
- American Chemical Society
- Year
- 1992
- Tongue
- English
- Weight
- 473 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0022-3263
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๐ SIMILAR VOLUMES
The highly stereoselective synthesis of (1S,2S)-2-amino-1-hydroxyalkylphosphonic acids was achieved by addition of dimethyl phosphite to N-protected aminoaldehydes. Relative configuration and solution conformations of (1S,2S)-2-amino-1hydroxy-alkylphosphonic acids (in D 2 O) and their dimethyl ester
Synthesis of (2S)-2-Amino-3-(1H-4-indolyl)propanoic Acid, a Novel Tryptophan Analogue for Structural Modification of Bioactive Peptides. -A new and multigram synthesis of title compound (VIIIa) uses a Schoellkopf chiral auxiliary reagent in the key step. The protected derivative (VIIIb) can be read
The synthesis of a pseudo-tripeptide 9 and a pseudo-pontapoptide 1 incorporating the conformationally constrained 13-amino acid (2S,3R)-2-amino cyclopropane earbox'ylic acid is reported. The key steps of the ~'nthesis are the desynmletrisation of cyclopropane 1,2-dicarbox'ylic anhydride using (S)-pr