Synthesis and characterisation of O-6-alkylthio- and perfluoroalkylpropanethio-α-cyclodextrins and their O-2-, O-3-methylated analogues
Synthesis and characterisation of O-6-alkylthio- and perfluoroalkylpropanethio-α-cyclodextrins and their O-2-, O-3-methylated analogues
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DOI:
10.1039/b703894a
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发表时间:
2007-01-01
影响因子:
3.3
通讯作者:
Parrot-Lopez, Hélène
中科院分区:
文献类型:
--
作者:
Ghera, Bernard Bertino;Perret, Florent;Parrot-Lopez, Hélène
The synthesis of twelve alkylthio- or per. uoroalkylpropanethio-alpha-cyclodextrin derivatives and their O-2-, O-3-methylated analogues are described. The coupling reaction involves firstly the basic in situ hydrolysis of alkylperfluoropropane isothiouronium iodide or alkylisothiouronium bromide, then reaction with an alpha-cyclodextrin modified at the C-6 position by an iodine or methylsulfonyl group. The interfacial properties of these new compounds have been determined by the studies of their mono-molecular layer at the air-water interface.