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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

C_2-symmetric BINOL-squaramide as efficient organocatalyst for the enantioselective α-amination of 1,3-dicarbonyl compounds with dialkyl azodicarboxylates
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摘要 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). 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).
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2015年第6期744-748,共5页 中国化学快报(英文版)
基金 the Fundamental Research Funds for the Central Universities (No.2042014kf0248) for support of this research
关键词 Asymmetric amination 1 3-Dicarbonyl compound Dialkyl azodicarboxylates Asymmetric amination 1,3-Dicarbonyl compound Dialkyl azodicarboxylates
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