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The first synthesis of optically active 1-substituted taurines
Xu, JX ; Xu, S ; Zhang, QH
刊名heteroatom chemistry
2005
关键词TRANSITION-STATE ISOSTERE SOLID-PHASE SYNTHESIS ASYMMETRIC-SYNTHESIS MITSUNOBU REACTION ACIDS SULFINAMIDE SULFONOPEPTIDES PEPTIDES
DOI10.1002/hc.20133
英文摘要Optically active 1-substituted taurines, a type of important sulfur analogues of naturally occurring amino acids, and their N-benzyloxycarbonyl-protected derivatives were synthesized from the corresponding optically active beta-amino secondary alcohols in three steps via N-protection with benzyl chloroformate, substitution with thiolacetic acid under Mitsunobu conditions, and oxidation with performic acid. (c) 2005 Wiley Periodicals, Inc.; Chemistry, Multidisciplinary; SCI(E); EI; 14; ARTICLE; 6; 466-471; 16
语种英语
内容类型期刊论文
源URL[http://ir.pku.edu.cn/handle/20.500.11897/151597]  
专题化学与分子工程学院
推荐引用方式
GB/T 7714
Xu, JX,Xu, S,Zhang, QH. The first synthesis of optically active 1-substituted taurines[J]. heteroatom chemistry,2005.
APA Xu, JX,Xu, S,&Zhang, QH.(2005).The first synthesis of optically active 1-substituted taurines.heteroatom chemistry.
MLA Xu, JX,et al."The first synthesis of optically active 1-substituted taurines".heteroatom chemistry (2005).
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