Hydrogenation of 4-deoxy-beta-L-threo-hex-4-enopyranosyluronic acid sodiumsalt attached to xylodiose or xylotriose

Citation
Sa. Selkala et al., Hydrogenation of 4-deoxy-beta-L-threo-hex-4-enopyranosyluronic acid sodiumsalt attached to xylodiose or xylotriose, TETRAHEDR L, 42(18), 2001, pp. 3215-3217
Citations number
9
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
42
Issue
18
Year of publication
2001
Pages
3215 - 3217
Database
ISI
SICI code
0040-4039(20010430)42:18<3215:HO4AS>2.0.ZU;2-T
Abstract
A sodium salt of 4-deoxy-beta -L-threo-hex-4-enopyranosyluronic acid 1 atta ched to xylodiose or xylotriose is hydrogenated for the first time. Moreove r, the double bond of 4-deoxy-beta -L-threo-hex-4-enopyranosyluronic acid s odium salt 1 can be reduced by hydrogenation in water without removing the allylic hydroxyl group. Highly active homogeneous catalysts and heterogeneo us catalysts were tested and only palladium or platinum on charcoal catalys ts were found to be active in this case. (C) 2001 Elsevier Science Ltd. AH rights reserved.