1997
DOI: 10.1016/s0014-3057(96)00169-3
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Linear Cyclodextrin-Poly(vinylamine): Synthesis and NMR Characterization

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Cited by 25 publications
(13 citation statements)
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“…[13] An amount of 0.75 g of tosyl chloride was added to 60 ml of anhydrous pyridine solution containing 9 g of bCD. The mixture was stirred for 48 hours at 0 C in an ice bath.…”
Section: Preparation Of Polyethyleneimine Grafting B-cyclodextrin (Pementioning
confidence: 99%
“…[13] An amount of 0.75 g of tosyl chloride was added to 60 ml of anhydrous pyridine solution containing 9 g of bCD. The mixture was stirred for 48 hours at 0 C in an ice bath.…”
Section: Preparation Of Polyethyleneimine Grafting B-cyclodextrin (Pementioning
confidence: 99%
“…␤CD was tosylated by reacting ␤CD and tosyl chloride, following a method reported elsewhere [20]. Tosyl chloride, 0.75 g, was added to 60 ml of ␤CD solution in anhydrous pyridine (15%, w/v).…”
Section: Preparation Ofˇ-cyclodextrin Grafted Polyethyleneimine (Pei-mentioning
confidence: 99%
“…This substitution reaction on 9b with a polymeric nucleophile has been applied more often, though with different polymers. As well as poly (allylamine) [28,[33][34][35], poly(vinylamine) [36][37][38][39][40], linear [38] and branched poly (ethylenimine) [38][39][40] and poly(ethylene glycol-block-aspartamide) [41] were used. However, for polymers which do not contain highly nucleophilic amino groups, other strategies had to be developed.…”
Section: Polymer-analogous Reaction With Monofunctional Cyclodextrinmentioning
confidence: 99%