Novel approaches to glycopolymer syntheses from the viewpoint of polymerization chemistry

Citation
J. Kadokawa et al., Novel approaches to glycopolymer syntheses from the viewpoint of polymerization chemistry, SYNLETT, (12), 1999, pp. 1845-1856
Citations number
52
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNLETT
ISSN journal
09365214 → ACNP
Issue
12
Year of publication
1999
Pages
1845 - 1856
Database
ISI
SICI code
0936-5214(199912):12<1845:NATGSF>2.0.ZU;2-F
Abstract
The new approaches to glycopolymer syntheses are introduced from the viewpo int of classification into the general polymerization reactions, i.e., poly addition, polycondensation, and radical polymerization. The ring-opening po lyaddition of sugar oxazoline monomers having the hydroxy group gave stereo regular aminopolysaccharides. Hydroxy-terminated oligodihexanoylchitin was prepared and its block copolyaddition with the other hydroxy terminated pol ymer or oligomer was carried out using diisocyanate as a coupling reagent. The direct polycondensation of D-glucosamine derivatives using the appropri ate condensing agents proceeded at st primary hydroxy group of position 6 r egioselectively. Furthermore, spontaneous polycondenssttion of aminosacchar ide monomers gave new aminopolysaccharides having unique structures. Radica l alternating copolymerization of 1,2-dideoxysaccharide with maleic anhydri de took place using AIBN initiator.