LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
An Efficient Synthesis of Chiral Diamines with Rigid Backbones: Application in Enantioselective Michael Addition of Malonates to Nitroalkenes
Department羰基合成与选择氧化国家重点实验室
Zhu QM(朱其明); Huang HM(黄汉民); Shi DJ(史登健); Shen ZQ(沈志强); Xia CG(夏春谷)
2009
Source PublicationOrganic Letters
ISSN1523-7060
Volume11Issue:20Pages:4536-4539
AbstractA new and efficient route for synthesis of enantiomerically pure biisoindoline and its isomer based on the diaza-Cope rearrangement reaction with chiral 1,2-bis(2-hydroxylphenyl)-1,2-diaminoethane as starting material has been developed. The newly prepared biisoindoline was employed as a chiral ligand in the Ni(II)-catalyzed enantioselective Michael addition of malonates to conjugated nitroalkenes, and good to excellent enantioselectivities were obtained.
Subject Area清洁催化与生物转化
Funding Organizationthe National Natural Science Foundation of China (20802085;20625308)
Indexed BySCI
Language英语
Funding Project清洁催化与生物转化研究组
Citation statistics
Cited Times:50[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/528
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorHuang HM(黄汉民); Xia CG(夏春谷)
Recommended Citation
GB/T 7714
Zhu QM,Huang HM,Shi DJ,et al. An Efficient Synthesis of Chiral Diamines with Rigid Backbones: Application in Enantioselective Michael Addition of Malonates to Nitroalkenes[J]. Organic Letters,2009,11(20):4536-4539.
APA 朱其明,黄汉民,史登健,沈志强,&夏春谷.(2009).An Efficient Synthesis of Chiral Diamines with Rigid Backbones: Application in Enantioselective Michael Addition of Malonates to Nitroalkenes.Organic Letters,11(20),4536-4539.
MLA 朱其明,et al."An Efficient Synthesis of Chiral Diamines with Rigid Backbones: Application in Enantioselective Michael Addition of Malonates to Nitroalkenes".Organic Letters 11.20(2009):4536-4539.
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