Synthesis of Orthogonally Protected Cyclic Homooligomers from Sugar Amino Acids
✍ Scribed by Ménand, Mickaël; Blais, Jean-Claude; Hamon, Louis; Valéry, Jean-Marc; Xie, Juan
- Book ID
- 126300302
- Publisher
- American Chemical Society
- Year
- 2005
- Tongue
- English
- Weight
- 252 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Two synthetic strategies for the generation of differentially protected, chiral tri-amino acids have been developed. The first strategy is based on the reductive amination of a serine-derived oxazolidine aldehyde with mono N-protected ethylenediamine. The second approach involves reductive alkylatio
The synthesis of four novel, "cationic", a,u-disubstituted amino acids is described. The new amino acids use an orthogonal protection scheme making them suitable for incorporation via solid-phase peptide synthesis.