Amino acid based diastereoselective synthesis of elsaminose
✍ Scribed by María Ruiz; Vicente Ojea; JoséMa Quintela
- Book ID
- 103411797
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- French
- Weight
- 274 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
As part of an ongoing project concerning the synthesis of deprotection and Boc-protection yielded the expected β 2amino acids. X-ray analysis of the alkylation product nonnatural amino acids, we have now developed a general strategy for the preparation of β 2 -amino acids (or 2-established that (Ϫ)-
l-Deoxygalactostatin (2) and (2S, 3S, 4R, 5S)-trihydroxypipecolic acid (15) have been synthesised from known building blocks derived from glycine, D-valine and L-tartaric acid (eight and seven steps, with 23% and 27% yield, respectively), via a syn-aldol reaction between 4-O-(tertbutyldiphenylsilyl)