1992
DOI: 10.1016/s0040-4039(00)61134-6
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Selective preparation of hexakis (6-O-arenesulfonyl) -α-cyclodextrin

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Cited by 9 publications
(1 citation statement)
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“…Nevertheless, factors such as steric crowding and complex formation decrease the yield as the degree of substitution increases. Sulfonylation with tosyl chloride is a good approach to perfunctionalize cyclodextrins, and has been applied to α- [ 133 ], β- [ 134 ], and γ- [ 135 ] cyclodextrins. Persulfonylated cyclodextrins are generally used as intermediates toward other functionalized CD derivatives.…”
Section: Functionalization Of Cyclodextrins: Synthetic Aspectsmentioning
confidence: 99%
“…Nevertheless, factors such as steric crowding and complex formation decrease the yield as the degree of substitution increases. Sulfonylation with tosyl chloride is a good approach to perfunctionalize cyclodextrins, and has been applied to α- [ 133 ], β- [ 134 ], and γ- [ 135 ] cyclodextrins. Persulfonylated cyclodextrins are generally used as intermediates toward other functionalized CD derivatives.…”
Section: Functionalization Of Cyclodextrins: Synthetic Aspectsmentioning
confidence: 99%