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
Chemo-Enzymatic Synthesis of (2 S ,4 R )-2-Amino-4-(3-(2,2-diphenylethylamino)-3-oxopropyl)pentanedioic Acid: A Novel Selective Inhibitor of Human Excitatory Amino Acid Transporter Subtype 2
✍ Scribed by Sagot, Emanuelle; Jensen, Anders A.; Pickering, Darryl S.; Pu, Xiaosui; Umberti, Michelle; Stensbøl, Tine B.; Nielsen, Birgitte; Assaf, Zeinab; Aboab, Bétina; Bolte, Jean; Gefflaut, Thierry; Bunch, Lennart
- Book ID
- 120604104
- Publisher
- American Chemical Society
- Year
- 2008
- Tongue
- English
- Weight
- 320 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0022-2623
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📜 SIMILAR VOLUMES
2S,3S,4R)-4-Amino-3-hydroxy-2-methylpentanoic acid has been synthesized through acylation of a chiral enolate and subsequent stereoselective reduction.
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