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A reliable synthesis of 2- and 6-amino-β-cyclodextrin and permethylated-β-cyclodextrin
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摘要
A new, reliable method for the introduction of an amine group at positions 2 or 6 of β-cyclodextrin and permethyl-β-cyclodextrin is described. It involves selective tosylation followed by azide substitution and almost quantitative reduction with triphenylphosphine followed by hydrolysis of the phosphinimine intermediate.

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