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学科主题: 天然产物有机化学
题名: Catalytic Enantioselective Synthesis of Chiral Phthalides by Efficient Reductive Cyclization of 2-Acylarylcarboxylates under Aqueous Transfer Hydrogenation Conditions
其他题名: Catalytic Enantioselective Synthesis of Chiral Phthalides by Efficient Reductive Cyclization of 2-Acylarylcarboxylates under Aqueous Transfer Hydrogenation Conditions
作者: Zhang B(张波) ; Xu MH(徐明华) ; Lin GQ(林国强)
通讯作者: 徐明华 ; 林国强
刊名: Org. Lett.
发表日期: 2009-01-01
卷: 11, 期:20, 页:4712-4715
收录类别: SCI
部门归属: 上海有机所; 上海药物所
英文摘要: A new diamine ligand for asymmetric transfer hydrogenation (ATH) was discovered, The reductive cyclization of 2-acylarylcarboxylates was found to proceed highly stereoselectively by the new Ru complex-catalyzed ATH and subsequent in situ lactonization under aqueous conditions. It enables efficient access to a wide variety of 3-substituted phthalides in enantiomerically pure form.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000270461300058
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/16691
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:
Zhang B,Xu MH,Lin GQ. Catalytic Enantioselective Synthesis of Chiral Phthalides by Efficient Reductive Cyclization of 2-Acylarylcarboxylates under Aqueous Transfer Hydrogenation Conditions[J]. Org. Lett.,2009,11(20):4712-4715.
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