中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Palladium-catalyzed N-arylsulfonamide formation from arylsulfonyl hydrazides and nitroarenes

文献类型:期刊论文

作者Zhao, Feng1; Li, Bin1; Huang, Huawen1; Deng, Guo-Jun1,2
刊名RSC ADVANCES
出版日期2016
卷号6期号:16页码:13010-13013
英文摘要A palladium-catalyzed construction for N-arylsulfonamide from nitroarenes and arylsulfonyl hydrazides is developed. In this protocol, abundant and stable nitroarenes serve as the nitrogen sources by in situ reduction reaction of hydrogen released from arylsulfonyl hydrazides. No external oxidants or reductants are needed for this kind of transformation.
收录类别SCI
语种英语
公开日期2016-05-03
源URL[http://ir.iccas.ac.cn/handle/121111/30118]  
专题化学研究所_分子识别与功能实验室
作者单位1.Xiangtan Univ, Coll Chem, Minist Educ, Key Lab Environm Friendly Chem & Applicat, Xiangtan 411105, Peoples R China
2.Chinese Acad Sci, Inst Chem, Key Lab Mol Recognit & Funct, Beijing 100080, Peoples R China
推荐引用方式
GB/T 7714
Zhao, Feng,Li, Bin,Huang, Huawen,et al. Palladium-catalyzed N-arylsulfonamide formation from arylsulfonyl hydrazides and nitroarenes[J]. RSC ADVANCES,2016,6(16):13010-13013.
APA Zhao, Feng,Li, Bin,Huang, Huawen,&Deng, Guo-Jun.(2016).Palladium-catalyzed N-arylsulfonamide formation from arylsulfonyl hydrazides and nitroarenes.RSC ADVANCES,6(16),13010-13013.
MLA Zhao, Feng,et al."Palladium-catalyzed N-arylsulfonamide formation from arylsulfonyl hydrazides and nitroarenes".RSC ADVANCES 6.16(2016):13010-13013.

入库方式: OAI收割

来源:化学研究所

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