中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Synthesis of alpha-Aryl Esters and Nitriles: Deaminative Coupling of alpha-Aminoesters and alpha-Aminoacetonitriles with Arylboronic Acids

文献类型:期刊论文

作者Wu, Guojiao1,2; Deng, Yifan1,2; Wu, Chaoqiang1,2; Zhang, Yan1,2; Wang, Jianbo1,2,3
刊名ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
出版日期2014-09-22
卷号53期号:39页码:10510-10514
关键词Arenes Boron Diazo Compounds Nitriles Synthetic Methods
ISSN号1433-7851
DOI10.1002/anie.201406765
英文摘要Transition-metal-free synthesis of alpha-aryl esters and nitriles using arylboronic acids with alpha-aminoesters and alpha-aminoacetonitriles, respectively, as the starting materials has been developed. The reaction represents a rare case of converting C(sp(3)) N bonds into C(sp(3)) C(sp(2)) bonds. The reaction conditions are mild, demonstrate good functional-group tolerance, and can be scaled up.
语种英语
WOS记录号WOS:000342760700044
出版者WILEY-V C H VERLAG GMBH
源URL[http://ir.iccas.ac.cn/handle/121111/50867]  
专题中国科学院化学研究所
通讯作者Wang, Jianbo
作者单位1.Peking Univ, Coll Chem, BNLMS, Beijing 100871, Peoples R China
2.Peking Univ, Coll Chem, Minist Educ, Key Lab Bioorgan Chem & Mol Engn, Beijing 100871, Peoples R China
3.Chinese Acad Sci, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
推荐引用方式
GB/T 7714
Wu, Guojiao,Deng, Yifan,Wu, Chaoqiang,et al. Synthesis of alpha-Aryl Esters and Nitriles: Deaminative Coupling of alpha-Aminoesters and alpha-Aminoacetonitriles with Arylboronic Acids[J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION,2014,53(39):10510-10514.
APA Wu, Guojiao,Deng, Yifan,Wu, Chaoqiang,Zhang, Yan,&Wang, Jianbo.(2014).Synthesis of alpha-Aryl Esters and Nitriles: Deaminative Coupling of alpha-Aminoesters and alpha-Aminoacetonitriles with Arylboronic Acids.ANGEWANDTE CHEMIE-INTERNATIONAL EDITION,53(39),10510-10514.
MLA Wu, Guojiao,et al."Synthesis of alpha-Aryl Esters and Nitriles: Deaminative Coupling of alpha-Aminoesters and alpha-Aminoacetonitriles with Arylboronic Acids".ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 53.39(2014):10510-10514.

入库方式: OAI收割

来源:化学研究所

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