Stereospecific synthesis of (2S,3R)-2-amino-3-mercaptobutyric acid - an intermediate for incorporation into .beta.-methyllanthionine-containing peptides
β Scribed by Morell, John L.; Fleckenstein, Peter; Gross, Erhard
- Book ID
- 118268779
- Publisher
- American Chemical Society
- Year
- 1977
- Tongue
- English
- Weight
- 318 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
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
A Facile Approach for the Synthesis of Pseudo-Peptides Incorporating a (2S,3R)-2-Amino-cyclopropane Carboxylic Acid Residue. -The new approach to the synthesis of the title compounds is based on the desymmetrization of meso-anhydride (I) followed by a Curtius rearrangement to obtain key building bl