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机构地区:[1]Department of Chemistry, Huazhong University of Science and Technology, Wuhan 430074, China
出 处:《Chinese Journal of Chemistry》2005年第10期1289-1291,共3页中国化学(英文版)
基 金:Project supported by the National Natural Science Foundation of China (No. 20072007).
摘 要:Chiral nitrogen-containing calix[4]arene was easily synthesized by the reaction of 25,27-di(2-bromoethoxy)- 26,28-dihydroxy-5,11,17,23-tetrakis(t-butyl)calix[4]arene with S-(-)-1-phenylethylamine in excellent yield, and showed good ability to recognize the enantiomers of mandelic acid and 2,3-dibenzoyltartaric acid. This finding has potential application to assay and separation of enantiomers of the carboxylic acids.Chiral nitrogen-containing calix[4]arene was easily synthesized by the reaction of 25,27-di(2-bromoethoxy)- 26,28-dihydroxy-5,11,17,23-tetrakis(t-butyl)calix[4]arene with S-(-)-1-phenylethylamine in excellent yield, and showed good ability to recognize the enantiomers of mandelic acid and 2,3-dibenzoyltartaric acid. This finding has potential application to assay and separation of enantiomers of the carboxylic acids.
关 键 词:chiral nitrogen-containing arene chiral recognition carboxylic acid.
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