## Abstract Ring‐opening polymerization of anhtydro sugar derivatives was carried out with Lewis acid catalysts to produce block copolysaccharides. Polymerization of 1,4‐anhydro‐2,3‐di__O__‐__tert__‐butyldimethylsilyl‐α‐D‐ribopyranose (ADSR) with boron trifluoride etherate proceeded linearly and ra
Synthesis of Hyperbranched Carbohydrate Polymers by Ring-Opening Multibranching Polymerization of Anhydro Sugar
✍ Scribed by Toshifumi Satoh; Toyoji Kakuchi
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 232 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1616-5187
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✦ Synopsis
Abstract
The synthesis of novel hyperbranched carbohydrate polymers, prepared by the ring‐opening multibranching polymerizations of anhydro and dianhydro sugars, is described. The hyperbranched carbohydrate polymers were formed by the cationic polymerization of 1,6‐anhydro‐β‐D‐hexopyranose, 1,4‐anhydrotetritol, 2,3‐anhydrotetritol, and 1,2:5,6‐dianhydro‐D‐mannitol. These polymerizations proceeded without gelation to produce water‐soluble hyperbranched carbohydrate polymers with controlled molecular weights and narrow polydispersities. The values for the degree of branching of the polymers were in the range of 0.28–0.50. The polymerization method, which proceeds through a ring‐opening reaction by a proton‐transfer reaction mechanism, is a facile method leading to a spherical carbohydrate polymer with a high degree of branching.
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📜 SIMILAR VOLUMES
Three new 1,4-anhydro-glucopyranose derivatives having different hydroxyl protective groups such as 1,4-anhydro-2,3,6-tri-O-methyl-a-D-glucopyranose (AMGLU), 1,4-anhydro-6-O-benzyl-2,3-di-O-methyl-a-D-glucopyranose (A6BMG), and 1,4-anhydro-2,3-di-O-methyl-6-O-trityl-a-D-glucopyranose (A6TMG) were sy
## Abstract Ring‐opening metathesis polymerization has been used to prepare a series of water soluble polymers based on the Diels‐Alder adducts of furan and cyclopentadiene. Hydrophobically modified forms of these polymers were obtained either by copolymerization with 5‐decylbicyclo[2.2.1]hept‐2‐en