Stereoselective Synthesis of the Nonproteinogenic Amino Acid (2 S ,3 R )-3-Amino-2-hydroxydecanoic Acid from (4 S ,5 S )-4-Formyl-5-vinyl-2-oxazolidinone
β Scribed by Wee, Andrew G. H.; McLeod, Douglas D.
- Book ID
- 125892927
- Publisher
- American Chemical Society
- Year
- 2003
- Tongue
- English
- Weight
- 180 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Taking advantage of the high functionality of an enantiopure protected syn-2R-amino-l,3,4-triol derivative, easily available on a multigram scale from Disoascorbic acid, several biologically active compounds have been synthesized such as the (2S,3R)-3-amino-2-hydroxydecanoic acid (AHDA), the N-termi
## 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 βFull Textβ option. The original article is trackable v
2S,3S,4R)-4-Amino-3-hydroxy-2-methylpentanoic acid has been synthesized through acylation of a chiral enolate and subsequent stereoselective reduction.