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学科主题: 生命有机化学
题名: Enantioselective synthesis of functionalized α-amino acids via a chiral guanidine catalyzed Michael addition reaction
其他题名: 通过手性胍催化的Michael加成反应来合成手性的官能化的α氨基酸
作者: Ma DW(马大为) ; Cheng KJ(成克军)
通讯作者: 马大为
刊名: Tetrahedron-Asymmetry
发表日期: 1999-01-01
卷: 10, 页:713-719
收录类别: SCI
部门归属: 中国科学院上海有机化学研究所生命有机化学国家重点实验室
英文摘要: Several chiral guanidines were evaluated as catalysts for the Michael reaction of glycine derivatives 7 with acrylic esters 8. The best result (30.4% ee) was obtained when 7b was reacted with 8b under the catalysis of guanidine 1 in THF.
语种: 英语
相关网址: 查看原文
内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/15353
Appears in Collections:生命有机化学国家重点实验室_期刊论文

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Recommended Citation:
Ma DW,Cheng KJ. Enantioselective synthesis of functionalized α-amino acids via a chiral guanidine catalyzed Michael addition reaction[J]. Tetrahedron-Asymmetry,1999,10:713-719.
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