A click chemistry-based “grafting through” approach to the synthesis of a biorelevant polymer brush
✍ Scribed by Cappelli, A.; Paolino, M.; Grisci, G.; Giuliani, G.; Donati, A.; Mendichi, R.; Boccia, A. C.; Samperi, F.; Battiato, S.; Paccagnini, E.; Giacomello, E.; Sorrentino, V.; Licciardi, M.; Giammona, G.; Vomero, S.
- Book ID
- 120397943
- Publisher
- The Royal Society of Chemistry
- Year
- 2011
- Tongue
- English
- Weight
- 578 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1759-9954
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📜 SIMILAR VOLUMES
## Abstract A versatile approach based on click chemistry to synthesize polyphosphazene glycopolymers is presented. The glucose‐substituted polyphosphazene was synthesized by nucleophilic substitution of poly(dichlorophosphazene) with propargylamine and the subsequent azide/alkyne “click” reaction
Different thymidine derivatives bearing either an iodoaryl moiety at the 5 0 position or a dialkylsilyl group at the 3 0 position have been efficiently synthesized as precursors for carbon-11 or fluorine-18 labeling, respectively. Furthermore, iodoarylated thymidine derivatives have been incorporate