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C_2-symmetric BINOL-squaramide as efficient organocatalyst for the enantioselective α-amination of 1,3-dicarbonyl compounds with dialkyl azodicarboxylates
引用本文:Shi Tang,Zhi-yong Wang,Bin Liu,Chun-E. Dong. C_2-symmetric BINOL-squaramide as efficient organocatalyst for the enantioselective α-amination of 1,3-dicarbonyl compounds with dialkyl azodicarboxylates[J]. 中国化学快报, 2015, 26(6): 744-748. DOI: 10.1016/j.cclet.2015.03.033
作者姓名:Shi Tang  Zhi-yong Wang  Bin Liu  Chun-E. Dong
作者单位:State Key Laboratory of Virology, Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (Wuhan University), Ministry of Education, Wuhan University School of Pharmaceutical Sciences, Wuhan 430071, China
基金项目:We are grateful to the Fundamental Research Funds for the Central Universities (No. 2042014kf0248) for support of this research.
摘    要:

收稿时间:2014-12-17
修稿时间:2015-03-05

C2-symmetric BINOL-squaramide as efficient organocatalyst for the enantioselective α-amination of 1,3-dicarbonyl compounds with dialkyl azodicarboxylates
Shi Tang,Zhi-yong Wang,Bin Liu,Chun-E. Dong. C2-symmetric BINOL-squaramide as efficient organocatalyst for the enantioselective α-amination of 1,3-dicarbonyl compounds with dialkyl azodicarboxylates[J]. Chinese Chemical Letters, 2015, 26(6): 744-748. DOI: 10.1016/j.cclet.2015.03.033
Authors:Shi Tang  Zhi-yong Wang  Bin Liu  Chun-E. Dong
Affiliation:State Key Laboratory of Virology, Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (Wuhan University), Ministry of Education, Wuhan University School of Pharmaceutical Sciences, Wuhan 430071, China
Abstract:The asymmetric α-amination of 1,3-dicarbonyl compounds with dialkyl azodicarboxylates has been achieved by C2-symmetric BINOL-squaramide bearing multiple hydrogen bond donors to provide the desired products in excellent yields and enantioselectivities (up to 99% yield and 98% ee).
Keywords:Asymmetric amination  1,3-Dicarbonyl compound  Dialkyl azodicarboxylates
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