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An expeditious synthesis of 1-substituted and cyclic taurines
Huang, JX ; Wang, F ; Du, DM ; Xu, JX
刊名synthesis stuttgart
2005
关键词amino acid aminoalkanesulfonic acid epoxide episulfide synthesis taurine TRANSITION-STATE ISOSTERE SOLID-PHASE SYNTHESIS ASYMMETRIC-SYNTHESIS BUILDING-BLOCKS ACID SULFONOPEPTIDES SULFINAMIDE HYDROLYSIS ANALOGS ESTERS
DOI10.1055/s-2005-869994
英文摘要A series of 1-substituted taurines, including optically active taurines, were synthesized expeditiously from epoxides via episulfidation with potassium sulfocyanate, ring-opening with dibenzylamine, followed by oxidation with performic acid, and hydrogenolysis in the presence of palladium hydroxide on carbon powder. This method was also used for the synthesis of trans-cyclic taurines.; Chemistry, Organic; SCI(E); EI; 28; ARTICLE; 13; 2122-2128
语种英语
内容类型期刊论文
源URL[http://ir.pku.edu.cn/handle/20.500.11897/399184]  
专题化学与分子工程学院
推荐引用方式
GB/T 7714
Huang, JX,Wang, F,Du, DM,et al. An expeditious synthesis of 1-substituted and cyclic taurines[J]. synthesis stuttgart,2005.
APA Huang, JX,Wang, F,Du, DM,&Xu, JX.(2005).An expeditious synthesis of 1-substituted and cyclic taurines.synthesis stuttgart.
MLA Huang, JX,et al."An expeditious synthesis of 1-substituted and cyclic taurines".synthesis stuttgart (2005).
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