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Chiral guanidine catalyzed Michael addition reaction and Diels-Alder reaction of anthrone and N-methylmaleimide
Alternative Title手性胍催化的蒽酮与甲基马来酰胺的Diels-Alder反应
Peng B(彭斌); Cheng KJ(成克军); Ma DW(马大为)
2000
Source PublicationChin. J. Chem.
ISSN1001-604X
Volume18Issue:3Pages:411-413
AbstractTwo 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℃.
Subject Area有机化学
Department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
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Indexed BySCI
Language英语
WOS IDWOS:000087546400027
Citation statistics
Cited Times:11[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/15377
Collection生命有机化学国家重点实验室
Corresponding AuthorMa DW(马大为)
Recommended Citation
GB/T 7714
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.
APA 彭斌,成克军,&马大为.(2000).Chiral guanidine catalyzed Michael addition reaction and Diels-Alder reaction of anthrone and N-methylmaleimide.Chin. J. Chem.,18(3),411-413.
MLA 彭斌,et al."Chiral guanidine catalyzed Michael addition reaction and Diels-Alder reaction of anthrone and N-methylmaleimide".Chin. J. Chem. 18.3(2000):411-413.
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