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学科主题: 天然产物有机化学
题名: Organocatalyzed enantioselective one-pot three-component access to indoloquinolizidines by a Michael addition-Pictet-Spengler sequence
其他题名: Organocatalyzed enantioselective one-pot three-component access to indoloquinolizidines by a Michael addition-Pictet-Spengler sequence
作者: Wu XY(吴小余) ; Dai XY(戴小鸯) ; Nie LL(聂凛凛) ; Fang HH(房辉辉) ; Chen J(陈结) ; REN ZHONGJIAO ; Cao WG(曹卫国) ; Zhao G(赵刚)
通讯作者: 赵刚
刊名: Chem. Commun.
发表日期: 2010
卷: 46, 期:16, 页:2733-2735
收录类别: SCI
部门归属: 上海大学; 中国科学院上海有机化学研究所
英文摘要: The enantioselective three-component Michael addition-Pictet-Spengler sequence of beta-ketoesters 1, alpha,beta-unsaturated aldehydes 2 and tryptamines 4 represents a facile and rapid one-pot access to highly substituted indoloquinolizidines in moderate to excellent yields and good to excellent enantioselectivities.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000276376000005
Citation statistics:
内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/20797
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:
Wu XY,Dai XY,Nie LL,et al. Organocatalyzed enantioselective one-pot three-component access to indoloquinolizidines by a Michael addition-Pictet-Spengler sequence[J]. Chem. Commun.,2010,46(16):2733-2735.
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