𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of (2S*,4R*,5S*)-Piperidinetricarboxylic Acid, a Non-proteinogenic Amino Acid Isolated from Clitocybe acromelalga

✍ Scribed by Shirahama, Haruhisa; Hashimoto, Kimiko; Higashibayashi, Shuhei


Book ID
121757760
Publisher
Japan Institute of Heterocyclic Chemistry
Year
1997
Tongue
English
Weight
254 KB
Volume
46
Category
Article
ISSN
0385-5414

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Synthesis of (2S*,4
✍ K. HASHIMOTO; S. HIGASHIBAYASHI; H. SHIRAHAMA πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 1 views

Synthesis of (2S\*,4R\*,5S\*)-Piperidinetricarboxylic Acid, a Non-Proteinogenic Amino Acid Isolated from Clitocybe Acromelalga. -The title compound (IX) is synthesized from the pyridine triester (VI) by stepwise hydrogenation of the pyridine ring with intermediate cis-trans isomerization. -(HASHIMO

Synthesis of (2S,3R)-3-amino-2-hydroxyde
✍ Arounarith Tuch; MichΓ¨le SaniΓ¨re; Yves Le Merrer; Jean-Claude Depezay πŸ“‚ Article πŸ“… 1996 πŸ› Elsevier Science 🌐 English βš– 528 KB

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