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dc.contributor.authorWang, Fang
dc.contributor.authorHe, Wen-Bin
dc.contributor.authorWang, Jin-He
dc.contributor.authorYan, Xiao-Sheng
dc.contributor.authorZhan, Ying
dc.contributor.authorMa, Ying-Ying( Southwest Univ, Coll Chem & Chem Engn)
dc.contributor.authorYe, Li-Cai
dc.contributor.authorYang, Rui( Southwest Univ, Coll Chem & Chem Engn)
dc.contributor.authorCai, Fu
dc.contributor.authorLi, Zhao
dc.contributor.authorJiang, Yun-Bao
dc.contributor.author江云宝
dc.date.accessioned2012-03-29T01:24:05Z
dc.date.available2012-03-29T01:24:05Z
dc.date.issued2011-09-30
dc.identifier.citationCHEMICAL COMMUNICATIONS,2011,47(42):11784-11786zh_CN
dc.identifier.issn1359-7345
dc.identifier.urihttp://dx.doi.org/doi:10.1039/c1cc14995d
dc.identifier.uriWOS:000296020200061
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/11913
dc.description.abstractN-Amidothioureas generated from amine-dimethylated natural L-phenylalanine and its D-enantiomer bearing a chiral carbon that is by 2 atoms or 3 chemical bonds away from the anion binding site establish chiral communication upon acetate anion binding to the thiourea moiety.zh_CN
dc.description.sponsorshipNSFC[20835005, J1030415]; MOST of China[2011CB910403]zh_CN
dc.language.isoenzh_CN
dc.publisherROYAL SOC CHEMISTRYzh_CN
dc.titleAmino acid based chiral N-amidothioureas. Acetate anion binding induced chirality transferzh_CN
dc.typeArticlezh_CN


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