Meta/para-selectivity variation by sulfide/sulfoxide conversion of 6-substituted β-cyclodextrin. Hydrolyses of nitrophenyl acetates. ag |
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Authors: | Kahee Fujita Seiji Ejima Tadashi Ueda Taiji Imoto Hans-Rolf Schulten |
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Institution: | 1. Faculty of Pharmaceutical Sciences, Kyushu University 62 Maidashi, Higashi-ku, Fukuoka 812, Japan |
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Abstract: | Hydrolyses of m- and p-nitrophenyl acetates by 6-deoxy-6-alkylthio-β-cyclodextrins and the corresponding sulfoxides were studied to show that the small chemical conversion from the sulfides to the sulfoxides led to a change of meta/para-selectivity in the hydrolysis of the β-cyclodextrin moiety. |
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