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Copper-Catalyzed Enantioselective 1,6-Boration of para-Quinone Methides and Efficient Transformation of gem-Diarylmethine Boronates to Triarylmethanes

文献类型:期刊论文

作者Lou, Yazhou; Cao, Peng; Jia, Tao; Zhang, Yongling; Wang, Min; Liao, Jian
刊名ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
出版日期2015
卷号54期号:41页码:12134-12138
关键词CROSS-COUPLING REACTIONS ALPHA,BETA-UNSATURATED CARBONYL-COMPOUNDS ASYMMETRIC BETA-BORATION TERTIARY BORONIC ESTERS LITHIATION/BORYLATION-PROTODEBORONATION METHODOLOGY CONJUGATE ADDITIONS STEREOGENIC CENTERS CHIRAL SECONDARY 7-CYANO-7-ETHOXYCARBONYL-1,4-BENZOQUINONE METHIDE ANTIPROLIFERATIVE AGENTS
产权排序1
通讯作者Liao, J (reprint author), Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China.
合作状况国内
英文摘要Presented is the first enantioselective copper-catalyzed 1,6-conjugate addition of bis(pinacolato) diboron to para-quinone methides. The reaction proceeds with excellent yields and good to excellent enantioselectivities, and provides an attractive approach to the construction of optically active gem-diarylmehtine boronic esters. Additionally, the subsequent conversion of the derived potassium trifluoroborates into triarylmethanes with highly enantiospecificity was realized.
学科主题Chemistry
类目[WOS]Chemistry, Multidisciplinary
语种英语
源URL[http://210.75.237.14/handle/351003/27565]  
专题成都生物研究所_天然产物研究
推荐引用方式
GB/T 7714
Lou, Yazhou,Cao, Peng,Jia, Tao,et al. Copper-Catalyzed Enantioselective 1,6-Boration of para-Quinone Methides and Efficient Transformation of gem-Diarylmethine Boronates to Triarylmethanes[J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION,2015,54(41):12134-12138.
APA Lou, Yazhou,Cao, Peng,Jia, Tao,Zhang, Yongling,Wang, Min,&Liao, Jian.(2015).Copper-Catalyzed Enantioselective 1,6-Boration of para-Quinone Methides and Efficient Transformation of gem-Diarylmethine Boronates to Triarylmethanes.ANGEWANDTE CHEMIE-INTERNATIONAL EDITION,54(41),12134-12138.
MLA Lou, Yazhou,et al."Copper-Catalyzed Enantioselective 1,6-Boration of para-Quinone Methides and Efficient Transformation of gem-Diarylmethine Boronates to Triarylmethanes".ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 54.41(2015):12134-12138.

入库方式: OAI收割

来源:成都生物研究所

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