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学科主题: 天然产物有机化学
题名: Tandem intramolecular oxa-Michael addition/decarboxylation reaction catalyzed by bifunctional cinchona alkaloids: facile synthesis of chiral flavanone derivatives
其他题名: 双官能团金鸡纳碱催化的串联氧杂迈克尔加成/脱羧反应合成手性黄烷酮衍生物
作者: Wang HF(王海峰) ; Xiao H(肖华) ; Wang XW(王晓炜) ; Zhao G(赵刚)
通讯作者: 赵刚
刊名: Tetrahedron
发表日期: 2011
卷: 67, 期:30, 页:5389-5394
收录类别: SCI
部门归属: 中科院上海有机化学研究所; 中国科学技术大学
英文摘要: Bifunctional cinchona alkaloids were used to catalyze a tandem intramolecular oxa-Michael addition/decarboxylation reaction of alkylidene beta-ketoesters 1, providing a series of flavanone derivatives with up to 97% yield and 93% ee. (C) 2011 Elsevier Ltd. All rights reserved.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000292573700004
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/20819
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:
Wang HF,Xiao H,Wang XW,et al. Tandem intramolecular oxa-Michael addition/decarboxylation reaction catalyzed by bifunctional cinchona alkaloids: facile synthesis of chiral flavanone derivatives[J]. Tetrahedron,2011,67(30):5389-5394.
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