Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Yue-Jin Liu"'
Autor:
Yueliuting Fu, Cui-Hong Chen, Mao-Gui Huang, Jun-Yang Tao, Xu Peng, Hai-Bing Xu, Yue-Jin Liu, Ming-Hua Zeng
Publikováno v:
ACS Catalysis. 12:5036-5047
Autor:
Wen-Tao Ma, Mao-Gui Huang, Yueliuting Fu, Zhong-Hui Wang, Jun-Yang Tao, Jia-Wei Li, Yue-Jin Liu, Ming-Hua Zeng
Publikováno v:
Chemical Communications. 58:7152-7155
We report a phosphine-directed ruthenium-catalyzed C8-selective alkylation of naphthalenes with alkenes.
Publikováno v:
The Journal of Organic Chemistry. 86:11915-11925
Modification of commercially available biaryl monophosphine ligands via ruthenium(II)-catalyzed P(III)-directed-catalyzed ortho C-H secondary alkylation is described. The use of highly ring-strained norbornene as a secondary alkylating reagent is the
Publikováno v:
Advanced Synthesis & Catalysis. 363:2843-2849
Publikováno v:
Asian Journal of Organic Chemistry. 10:1113-1116
Autor:
Wen-Tao, Ma, Mao-Gui, Huang, Yueliuting, Fu, Zhong-Hui, Wang, Jun-Yang, Tao, Jia-Wei, Li, Yue-Jin, Liu, Ming-Hua, Zeng
Publikováno v:
Chemical communications (Cambridge, England). 58(51)
We report a phosphine-directed ruthenium-catalyzed C8-selective alkylation of naphthalenes with alkenes. This protocol provides straightforward access to a large library of electron-rich C8-alkyl substituent 1-naphthphosphines, which outperformed com
Publikováno v:
Organic Letters. 23:2057-2062
Herein, we disclose a ruthenium-catalyzed meta-selective C-H activation of phosphines by using intrinsic P(III) as a directing group. 2,2,6,6-Tetramethylheptane-3,5-dione acts as the ligand and exhibits an excellent performance in boosting the meta-a
Publikováno v:
Chinese Journal of Chemistry. 38:1545-1552
Publikováno v:
ACS Catalysis. 10:8212-8222
In the presence of accessible β-C–H bonds, γ-C–H activation of saturated aliphatic carboxamides remains unresolved because β-C–H activation is kinetically favored. This is almost a dogma in the dev...
Autor:
Ming-Hua Zeng, Mohamedally Kurmoo, Yue-Jin Liu, Rou-Ming Peng, Pan-Ting Tang, Yi Wei, Jia-Wei Li, Xiao-Peng Luo, Zheng-Xin Zhou, Abing Duan
Publikováno v:
Organic Letters. 22:4129-4134
Biphenylcarboxylic acid with two competing C(sp2)-H sites was designed for site selective C(sp2)-H functionalization by developing carboxylic acids assisted remote and selective olefination via 7-membered palladacycle. Mechanism investigation and DFT