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3-苯基异香豆冉酮衍生物的不对称Mannich反应研究

Study on the Mannich Reaction of 3-Phenyl Isocoumaranone Derivatives
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摘要 研究了双功能手性硫脲-叔胺催化剂催化的3-苯基异香豆冉酮衍生物与Ⅳ.保护亚胺的不对称Mannich反应,高收率、高对映选择性(88%-98%)地合成了一系列具有连续季碳叔碳手性中心的新化合物,其结构经1^H NMR和13^C NMR表征。 The asymmetric Mannich reaction of 3-phenyl i ne derivatives and N-protected imines were investigated using bifunctional thiourea-tertiary amine as the catalyst. A series of novel transformation afforded Mannich adducts bearing adjacent quaternary carbon and tertiary carbon chiral centers with high yield and excellent enantioselectivities (88% ee - 98% ee). The structures were characterized by 1^H NMR and 13^C NMR.
作者 刘灏 蒋琳
出处 《合成化学》 CAS CSCD 北大核心 2010年第2期154-158,163,共6页 Chinese Journal of Synthetic Chemistry
关键词 不对称催化 3-苯基异香豆冉酮 衍生物 MANNICH反应 硫脲-叔胺催化剂 asymmetric catalysis 3-phenyl isocoumaranone derivative Mannich reaction thioureatertiary amine catalyst
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