Titlebook: Macro-Glycoligands; Methods and Protocol Xue-Long Sun Book 2016 Springer Science+Business Media New York 2016 Glycopolymer-nanoparticle con

審美家

書目名稱Macro-Glycoligands影響因子(影響力)




書目名稱Macro-Glycoligands影響因子(影響力)學(xué)科排名




書目名稱Macro-Glycoligands網(wǎng)絡(luò)公開度




書目名稱Macro-Glycoligands網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Macro-Glycoligands被引頻次




書目名稱Macro-Glycoligands被引頻次學(xué)科排名




書目名稱Macro-Glycoligands年度引用




書目名稱Macro-Glycoligands年度引用學(xué)科排名




書目名稱Macro-Glycoligands讀者反饋




書目名稱Macro-Glycoligands讀者反饋學(xué)科排名

輕推

receptors

Glycopolymers Prepared by Ring-Opening Metathesis Polymerization Followed by Glycoconjugation Using olymerization is followed by attachment of a linker and subsequent glycoconjugation via a triazole-forming azide-alkyne click reaction. The use of a protected amine-terminating agent allows for the attachment of a probe molecule such as a fluorescein dye. The syntheses of a neutral galactopolymer as

猛然一拉

Protecting-Group-Free Synthesis of Glycopolymers and Their Binding Assay with Lectin and Influenza Vbe a facile protecting-group-free synthetic approach to glycopolymers bearing oligosaccharides from free saccharides by direct azidation and click chemistry methods, followed by reversible addition-fragmentation chain transfer polymerization. This method can be applied not only to mono- and disaccha

obstruct

Carbohydrate-Based Initiators for the Cationic Ring-Opening Polymerization of 2-Ethyl-2-Oxazolinebiomedical applications according to their specific needs. This contribution describes the detailed methodology to functionalize poly(2-ethyl-2-oxazoline), a polymer with properties very similar to polyethylene glycol, in a stereo-selective manner with a range of carbohydrates that can serve as biol

Antarctic

Heterofunctional Glycopolypeptides by Combination of Thiol-Ene Chemistry and NCA Polymerizationonalization of polypeptides with suitable functional groups. Here we present a method for the in-situ functionalization and (co-) polymerization of allylglycine .-carboxyanhydride in a facile one-pot procedure, combining radical thiol-ene photochemistry and nucleophilic ring-opening polymerization t

厭惡

生氣地

Galactosylated Polymer Nano-objects by Polymerization-Induced Self-Assembly, Potential Drug Nanocarrization-induced self-assembly, especially RAFT aqueous dispersion polymerization is a unique method to prepare such polymer nanostructures, as it enables the preparation of very-well-defined morphologies at very high concentrations. Here we describe the implementation of PISA to the synthesis of gal

輕推

冥界三河

Surface Modification of Polydivinylbenzene Microspheres with a Fluorinated Glycopolymer Using Thiol-ified with polypentafluorostyrene chains utilizing surface-initiated atom transfer radical polymerization techniques. The hydrophobic fluoropolymer-coated microsphere was then converted to a hydrophilic biopolymer by performing thiol-halogen click chemistry between polypentafluorostyrene and 1-thio-