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学科主题: 有机化学
题名: Chiral guanidine catalyzed Michael addition reaction and Diels-Alder reaction of anthrone and N-methylmaleimide
其他题名: 手性胍催化的蒽酮与甲基马来酰胺的Diels-Alder反应
作者: Peng B(彭斌) ; Cheng KJ(成克军) ; Ma DW(马大为)
通讯作者: 马大为
刊名: Chin. J. Chem.
发表日期: 2000
卷: 18, 期:3, 页:411-413
收录类别: SCI
部门归属: 上海复旦大学; 中国科学院上海有机化学研究所生命有机国家开放实验室
英文摘要: Two chiral guanidines were evaluated as catalysts for the reaction of anthrone (1) with N-methylmaleimide (2). When guanidine 5 was used, the michael adduct 4 was isolated as a major product. The best enantioselectivity (70% ee) was obtained when the reaction was carried out in THF at -20℃.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000087546400027
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/15377
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:
Peng B,Cheng KJ,Ma DW. Chiral guanidine catalyzed Michael addition reaction and Diels-Alder reaction of anthrone and N-methylmaleimide[J]. Chin. J. Chem.,2000,18(3):411-413.
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