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Amino acid synthesis using (L)-pyroglutamic acid as a chiral starting material

✍ Scribed by Jack E. Baldwin; Tania Miranda; Mark Moloney; Tuncer Hokelek


Book ID
108372189
Publisher
Elsevier Science
Year
1989
Tongue
French
Weight
669 KB
Volume
45
Category
Article
ISSN
0040-4020

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πŸ“œ SIMILAR VOLUMES


(L)-pyroglutamic acid as a chiral starti
✍ Jack E. Baldwin; Mark G. Moloney; Sung Bo Shim πŸ“‚ Article πŸ“… 1991 πŸ› Elsevier Science 🌐 French βš– 122 KB

Elaboration of lactam (1). readily available from &)-pyroglutamic acid, provides access to a range of 2,4-and 2,3,4-substituted pyrrolidinones.

Novel synthesis of l-iduronic acid using
✍ Hiroshi Hinou; Hidehiro Kurosawa; Koji Matsuoka; Daiyo Terunuma; Hiroyoshi Kuzuh πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 French βš– 255 KB

For the preparation of L-iduronic acid, trehalose was converted into a derivative of a novel disaccharide, B-Lidopyranosyl I~-L-idopyranoside, through diastereoselective hydroboration of the 5, 5'-di-eno intermediate. The 6-and 6'-hydroxy groups were then oxidized in two steps to give a disaccharide

(S)-Pyroglutamic Acid, (S)-Malic Acid, a
✍ Martin Ostendorf; Jan DΔ³kink; Floris P. J. T. Rutjes; Henk Hiemstra πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 398 KB πŸ‘ 2 views

The synthesis of four enantiopure hydroxyamidines is amidine was obtained by coupling of an (S)-malic acid derived N-acyliminium ion with Ξ²-naphthol. The other described. One amidine was obtained from (S)-pyroglutamic acid. Its key step involved the addition of phenylmagnesium amidines were obtained