Transition-metal-free cascade reaction of alpha-halo-N-tosylhydrazones, indoles and arylboronic acids
Wu, Guojiao1; Deng, Yifan1; Luo, Haiqing1; Zhou, Junliang1; Li, Tianjiao1; Zhang, Yan1; Wang, Jianbo1,2
刊名CHEMICAL COMMUNICATIONS
2016
卷号52期号:30页码:5266-5268
ISSN号1359-7345
DOI10.1039/c6cc01750a
文献子类Article
英文摘要alpha-Halo-N-tosylhydrazones are employed as reagents for the formation of multiple carbon-carbon bonds in the three-component reactions. In this transformation, a strategy has been designed to generate the diazo intermediate by using a nucleophile to react with the azoalkene intermediate generated in situ from the alpha-halo-N-tosylhydrazone. The diazo intermediate thus generated further undergoes transition-metal-free C-C bond forming reaction with arylboronic acids.
WOS关键词SITU GENERATED 1,2-DIAZA-1,3-DIENES ; IN-SITU ; EFFICIENT SYNTHESIS ; CARBONYL-COMPOUNDS ; COUPLING REACTIONS ; BORONIC ACIDS ; AZOALKENES ; CARBENE ; CYCLOADDITION ; INSERTION
WOS研究方向Chemistry
语种英语
出版者ROYAL SOC CHEMISTRY
WOS记录号WOS:000373687400011
内容类型期刊论文
源URL[http://cas-ir.dicp.ac.cn/handle/321008/170720]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
通讯作者Wang, Jianbo
作者单位1.Peking Univ, Key Lab Bioorgan Chem & Mol Engn, Coll Chem, Minist Educ,BNLMS, Beijing 100871, Peoples R China
2.Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
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GB/T 7714
Wu, Guojiao,Deng, Yifan,Luo, Haiqing,et al. Transition-metal-free cascade reaction of alpha-halo-N-tosylhydrazones, indoles and arylboronic acids[J]. CHEMICAL COMMUNICATIONS,2016,52(30):5266-5268.
APA Wu, Guojiao.,Deng, Yifan.,Luo, Haiqing.,Zhou, Junliang.,Li, Tianjiao.,...&Wang, Jianbo.(2016).Transition-metal-free cascade reaction of alpha-halo-N-tosylhydrazones, indoles and arylboronic acids.CHEMICAL COMMUNICATIONS,52(30),5266-5268.
MLA Wu, Guojiao,et al."Transition-metal-free cascade reaction of alpha-halo-N-tosylhydrazones, indoles and arylboronic acids".CHEMICAL COMMUNICATIONS 52.30(2016):5266-5268.
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