56503-24-3Relevant academic research and scientific papers
The Regiospecific Mono Tosylation of Cyclodextrins
Onozuka, Shigeharu,Kojima, Masayoshi,Hattori, Kenjiro,Toda, Fujio
, p. 3221 - 3224 (1980)
α- and β-Cyclodextrins were tosylated with tosyl chloride in an alkaline solution.The products were confirmed to be monotosylated compounds, and the tosyl group was introduced at the C-3 position of one glucose unit of the cyclodextrin molecule.The 1:1 complex formation of cyclodextrin with tosyl chloride was observed spectrometrically.
Unraveling unidirectional threading of α-cyclodextrin in a [2]rotaxane through spin labeling approach
Casati, Costanza,Franchi, Paola,Pievo, Roberta,Mezzina, Elisabetta,Lucarini, Marco
, p. 19108 - 19117 (2013/01/15)
We present here the results of a CW-ESR investigation of a double spin labeled α-cyclodextrin-based [2]rotaxane that is characterized by the presence of nitroxide labels both at the wheel and at the dumbbell. This was accomplished by synthesizing a spin l
CONVENIENT PREPARATION AND EFFECTIVE SEPARATION OF THE C-2 AND C-3 TOSYLATES OF α-CYCLODEXTRIN
Fujita, Kahee,Nagamura, Satoru,Imoto, Taiji
, p. 5673 - 5676 (2007/10/02)
Secondary tosylates of α-cyclodextrin were conveniently prepared by the reaction of the cyclodextrin with tosyl chloride in alkaline water where pH of the mixture should be allowed to decrease as the proceeding of reaction, and were effectivelly separated by reversed-phase column chromatography.
