Amphiphilic block copolymers of vinyl ethers (VES) of the type -[CH2CH(OCH,CH,0 R)]. - [CH,CH(OiBu)]n -were synthesized by living cationic polymerization, where R is a I>-glucose residue, and m and n are the degrees of polymerization (m = 20-50; n = 11-89). To obtain them, sequential living block c
Controlled Synthesis of Amphiphilic Block Copolymers with Pendant N -Acetyl- d -glucosamine Residues by Living Cationic Polymerization and Their Interaction with WGA Lectin
โ Scribed by Yamada, Kenji; Minoda, Masahiko; Miyamoto, Takeaki
- Book ID
- 120418055
- Publisher
- American Chemical Society
- Year
- 1999
- Tongue
- English
- Weight
- 133 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0024-9297
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๐ SIMILAR VOLUMES
D-Glucosamine-containing glycopolymers with well-controlled structure were synthesized by living cationic polymerization. To this end, D-glucosamine-containing vinyl ether (VE) of the type [CH 2 |CH(OCH 2 CH 2 OR)] was prepared, where R denotes a 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimide-b-D-glucopyr
Amphiphilic block and statistical copolymers of vinyl ethers (VEs) with pendant glucose residues were synthesized by the living cationic polymerization of isobutyl VE (IBVE) and a VE carrying 1,2:5,6-di-O-isopropylidene-D-glucose (IpGlcVE), followed by deprotection. The block copolymer was prepared
## Abstract Amphiphilic block polymers of vinyl ethers (VEs). \documentclass{article}\pagestyle{empty}\begin{document}$\rlap{--} [{\rm CH}\_{\rm 2} {\rm CH}\left( {{\rm OCH}\_{\rm 2} {\rm CH}\_{\rm 2} {\rm NH}\_{\rm 2} } \right)\rlap{--} ]\_m \rlap{--} [{\rm CH}\_{\rm 2} {\rm CH}\left( {{\rm OR}}