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学科主题: 天然产物有机化学
题名: Enantioselective alkynylation of a prochiral ketone catalyzed by C^2-symmetric diamino diols
其他题名: C^2对称的双氨基二醇催化的潜手性酮的立体选择性炔化
作者: Jiang B(姜标) ; Feng Y(冯炎)
通讯作者: 姜标
刊名: Tetrahedron Lett.
发表日期: 2002-01-01
卷: 43, 期:16, 页:2975-2977
收录类别: SCI
部门归属: 中国科学院上海有机化学研究所金属有机化学开放实验室
英文摘要: C^2 Symmetric diamino diols were used as chiral ligands to induce the asymmetric addition of lithium acetylides to carbonyl groups. The enantiomeric excesses (up to 99% ee) depended on the structure of the acetylene.
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/331003/20175
Appears in Collections:中科院天然产物有机化学重点实验室_期刊论文

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Recommended Citation:
Jiang B,Feng Y. Enantioselective alkynylation of a prochiral ketone catalyzed by C^2-symmetric diamino diols[J]. Tetrahedron Lett.,2002,43(16):2975-2977.
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