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北京大学 [29]

上海有机化学研究所 [8]

上海药物研究所 [6]

新疆理化技术研究所 [4]

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厦门大学 [3]

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金属有机化学 [6]

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物理化学与绿色催化 [1]

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	Organozinc-Mediated Direct C-C Bond Formation via C-N Bond Cleavage of Ammonium Salts 期刊论文 CHEMISTRY-AN ASIAN JOURNAL, 2017, 卷号: 12, 期号: 19, 页码: 2554-2557 作者: Wang, Dong-Yu; Morimoto, Koki; Yang, Ze-Kun; Wang, Chao; Uchiyama, Masanobu 收藏 \| 浏览/下载：11/0 \| 提交时间：2019/01/08 chemoselectivity C-N bond cleavage cross-coupling organozinc single electron transfer
	Stereoselective addition of Grignard reagents to (2-methyl-5-tert-butyl)phenyl 1-thio-beta-D-ribopentodialdo-1,4-furanoside derivative 期刊论文 TETRAHEDRON, 2017, 卷号: 73, 期号: 16, 页码: 2290-2304 作者: Ren, Huanming; Xie, Wuchen; Xiong, Bing; Shen, Jingkang; Chen, Guohua 收藏 \| 浏览/下载：20/0 \| 提交时间：2019/01/08 Nucleophilic addition Stereoselective reaction Grignard reagents 5-C-Substituted ribofuranoside Mosher ester
	Deoxygenation of Ethers To Form Carbon-Carbon Bonds via Nickel Catalysis 期刊论文 JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2017 Cao, Zhi-Chao; Shi, Zhang-Jie 收藏 \| 浏览/下载：5/0 \| 提交时间：2017/12/03 CROSS-COUPLING REACTIONS C-O BONDS ARYL ETHERS ALKYL-HALIDES GRIGNARD-REAGENTS BENZYLIC ETHERS OXYGEN BONDS ENOL ETHERS CLEAVAGE ACTIVATION
	Nickel-Catalyzed Oxidative Coupling of Unactivated C(sp(3))-H Bonds in Aliphatic Amides with Terminal Alkynes 期刊论文 ORGANOMETALLICS, 2017 Luo, Fei-Xian; Cao, Zhi-Chao; Zhao, Hong-Wei; Wang, Ding; Zhang, Yun-Fei; Xu, Xing; Shi, Zhang-Jie 收藏 \| 浏览/下载：3/0 \| 提交时间：2017/12/03 C-H BONDS ALPHA-AMINO-ACIDS DECARBOXYLATIVE ALKYNYLATION ROOM-TEMPERATURE SONOGASHIRA REACTIONS TOLUENE DERIVATIVES GRIGNARD-REAGENTS CARBOXYLIC-ACIDS DIRECT ARYLATION ARYL HALIDES
	Mechanistic Study on Nickel-Catalyzed Silylation of Aryl Methyl Ethers 期刊论文 CHEMISTRY-A EUROPEAN JOURNAL, 2017, 卷号: Vol.23 No.68, 页码: 17249-17256 作者: Jiang,Julong; Wang,Bing; Zhang,Qi; Yu,Haizhu; Fu,Yao 收藏 \| 浏览/下载：3/0 \| 提交时间：2019/04/22 CROSS-COUPLING REACTIONS O BOND ACTIVATION CARBON-OXYGEN BONDS C-OME CLEAVAGE TRANSITION-ELEMENTS GRIGNARD-REAGENTS ENOL ETHERS NI ELECTROPHILES DENSITY
	Nickel catalyzed reduction of arenols under mild conditions 期刊论文 ORGANIC CHEMISTRY FRONTIERS, 2016 Shi, Wen-Juan; Li, Xiao-Lei; Li, Zhao-Wei; Shi, Zhang-Jie 收藏 \| 浏览/下载：8/0 \| 提交时间：2017/12/03 C-O BOND CROSS-COUPLING REACTIONS ARYL ETHERS DIRECTING GROUP SELECTIVE HYDROGENOLYSIS GRIGNARD-REAGENTS BIOLOGICAL EVALUATION ROOM-TEMPERATURE BENZYL ALCOHOLS METHYL ETHERS
	Mechanism of Ni-NHC Catalyzed Hydrogenolysis of Aryl Ethers: Roles of the Excess Base 期刊论文 ACS CATALYSIS, 2016 Xu, Liping; Chung, Lung Wa; Wu, Yun-Dong 收藏 \| 浏览/下载：6/0 \| 提交时间：2017/12/03 nickel N-heterocyclic carbene hydrogenolysis C-O activation biomass H-2 activation C-O BONDS CROSS-COUPLING REACTIONS TRANSITION-METAL CENTERS CARBON-CARBON BONDS OXIDATIVE ADDITION DENSITY FUNCTIONALS REDUCTIVE CLEAVAGE CHEMICAL-REACTIONS GRIGNARD-REAGENTS NICKEL-CATALYSTS
	Nickel- or Iron-Catalyzed Cross-Coupling of Aryl Carbamates with Arylsilanes 期刊论文 ADVANCED SYNTHESIS & CATALYSIS, 2016 Shi, Wen-Juan; Zhao, Hong-Wei; Wang, Yang; Cao, Zhi-Chao; Zhang, Li-Sheng; Yu, Da-Gang; Shi, Zhang-Jie 收藏 \| 浏览/下载：2/0 \| 提交时间：2017/12/04 arylsilanes carbamates C-O activation copper(II) fluoride (CuF2) Hiyama reaction C-O BOND CARBON-OXYGEN BONDS GRIGNARD-REAGENTS METHYL ETHERS MILD CONDITIONS H BONDS ORGANOSILICON REAGENTS ORGANOBORON COMPOUNDS ORGANOZINC REAGENTS PHENOL DERIVATIVES
	Practical Cross-Coupling between O-Based Electrophiles and Aryl Bromides via Ni Catalysis 期刊论文 ORGANIC LETTERS, 2016 Cao, Zhi-Chao; Luo, Qin-Yu; Shi, Zhang-Jie 收藏 \| 浏览/下载：2/0 \| 提交时间：2017/12/03 C-C BONDS GRIGNARD-REAGENTS ALKYL-HALIDES NICKEL CATALYSIS PHENOL DERIVATIVES REDUCTIVE CLEAVAGE BENZYLIC ETHERS ORGANIC HALIDES MILD CONDITIONS DIRECTING GROUP
	Alkylations of Arylboronic Acids including Difluoroethylation/Trifluoroethylation via Nickel-Catalyzed Suzuki Cross-Coupling Reaction 期刊论文 ADVANCED SYNTHESIS & CATALYSIS, 2015, 卷号: 357, 期号: 12, 页码: 2721-2727 作者: Zhang, Xiaofei; Yang, Chunhao 收藏 \| 浏览/下载：13/0 \| 提交时间：2019/01/08 C(sp(3))-C(sp(2)) bond formation 2,2-difluoroethylation nickel catalyst Suzuki cross-coupling 2,2,2-trifluoroethylation

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