2010
DOI: 10.1039/c0py00310g
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Synthesis of heterobifunctional poly(ethylene glycol)s by an acetal protection method

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Cited by 12 publications
(7 citation statements)
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“…A related initiator with an acid cleavable acetal group was used to prepare polyethers with a predefined, cleavable functionality. , When preparing PEG with this initiator, PEGs with adjustable degree of polymerization with labile acetal unit in the chain are accessible. In particular, this initiator enables the synthesis of cleavable PEG, as shown in Figure .…”
Section: Poly(alkylene Oxide) Structures: Innovative Polyether Struct...mentioning
confidence: 99%
“…A related initiator with an acid cleavable acetal group was used to prepare polyethers with a predefined, cleavable functionality. , When preparing PEG with this initiator, PEGs with adjustable degree of polymerization with labile acetal unit in the chain are accessible. In particular, this initiator enables the synthesis of cleavable PEG, as shown in Figure .…”
Section: Poly(alkylene Oxide) Structures: Innovative Polyether Struct...mentioning
confidence: 99%
“…PEG was first modified by introduction of an azide on one terminal group (Scheme 1). Synthetic strategies aimed to asymmetrically modify PEG are largely explored in the literature.In general, the reported methods suffers from a complex chemistry and/or low purity of the final product (Li and Chau, 2010;Szekely et al, 2014). The most common way to synthesize heterotelechelic PEG remains polymerization of ethylene oxide from different initiators (Cammas et al, 1995;Hiki and Kataoka, 2007;Ishii et al, 2005;Raynaud et al, 2009;Thompson et al, 2008).…”
Section: Synthetic Strategymentioning
confidence: 99%
“…1 The most common route to these hetero-bifunctional PEG relies on anionic polymerization of ethylene oxide from functional initiators followed by post-modification of the terminal hydroxyl group. [9][10][11][12][13][14] Other techniques include the modification of commercially available, but expensive, modified PEG molecules [15][16][17] or the sequential and unsymmetrical alteration of end hydroxyl groups of linear PEG. In particular, the use of tosylate activating groups was reported by Mahou and Wandrey 18 for the generation of diverse heterotelechelic PEG oligomers.…”
Section: Introductionmentioning
confidence: 99%