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dc.contributor.authorYuan-Ping Ruan
dc.contributor.author阮源萍
dc.contributor.authorBang-Guo Wei
dc.contributor.authorXiu-Qing Xu
dc.contributor.authorGang Liu
dc.contributor.authorDe-Sheng Yu
dc.contributor.authorLiang-Xian Liu
dc.contributor.authorPei-Qiang Huang
dc.contributor.author黄培强
dc.date.accessioned2011-10-20T14:54:06Z
dc.date.available2011-10-20T14:54:06Z
dc.date.issued2005-09
dc.identifier.citationCHIRALITY,2005,17(9):595-599zh_CN
dc.identifier.issn0899-0042
dc.identifier.urihttp://dx.doi.org/doi:10.1002/chir.20205
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/10968
dc.description.abstractAn analytical HPLC method using CHIREX (S)-LEU/(S)-alpha-NEA column was developed for the determination of the enantiomeric excesses of N-protected (S)-3-hydroxyglutarimides. Using this method, detailed studies on the base-promoted ring-expansion reaction of the amidolactones, derived from L-glutamic acid, were undertaken.zh_CN
dc.language.isoenzh_CN
dc.publisherWILEY-LISSzh_CN
dc.subjectN-protected 3-hydroxyglutarimidezh_CN
dc.subjectenantioseparationzh_CN
dc.subjectring expansionzh_CN
dc.subjectracemizationzh_CN
dc.subjecthigh performance liquid chromatographyzh_CN
dc.subjectamidolactonezh_CN
dc.titleDetailed studies on the enantioselective synthesis and HPLC enantioseparation of N-protected 3-hydroxyglutarimideszh_CN
dc.typeArticlezh_CN


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