Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Chun‐Yang He"'
Publikováno v:
Molecules, Vol 25, Iss 3, p 508 (2020)
Here, we describe a mild, catalyst-free and operationally-simple strategy for the direct fluoroalkylation of olefins driven by the photochemical activity of an electron donor−acceptor (EDA) complex between DMA and fluoroalkyl iodides. The significa
Externí odkaz:
https://doaj.org/article/758ab72674c544e0af0cfdf67e54c5ff
Autor:
Weipiao Li, Jiajun Gao, Ting Mao, Xuefei Li, An‐Jun Wang, Pan Wang, Hao‐Yang Wang, Chun‐Yang He
Publikováno v:
Advanced Synthesis & Catalysis. 365:1596-1601
Autor:
Maoling Tao, Lin‐Yuan Zeng, Weipiao Li, Guoliang Pu, Jia Jia, Qiuli Yao, Xuefei Li, Chun‐Yang He
Publikováno v:
Advanced Synthesis & Catalysis. 365:854-859
Autor:
Peng Guo, Maoling Tao, Wen-Wen Xu, An-Jun Wang, Weipiao Li, Qiuli Yao, Jie Tong, Chun-Yang He
Publikováno v:
Organic Letters. 24:2143-2148
Herein, the first example using commercially available 2-bromo-3,3,3-trifluoropropene (BTP) as a radical acceptor has been reported. Taking advantage of this strategy, a wide range of secondary trifluoromethylated alkyl bromides were synthesized in g
Autor:
Ting Mao, Weipiao Li, Xiao‐Xiao Liu, Haoyang Wang, Wen‐Yong Han, Jie Tong, Shi‐Ji Xiao, Liang Zhao, Chun‐Yang He
Publikováno v:
Advanced Synthesis & Catalysis.
Autor:
Nan-Wei Wan, Wenyong Han, Chun-Yang He, Yongzheng Chen, Yong-Chao Shao, Jia-Li Huang, Baodong Cui, An-Ni Wang, Wen-Wen Zhao
Publikováno v:
Organic Letters. 23:9256-9261
We present herein a visible-light-induced [3 + 2] cycloaddition of a hypervalent iodine(III) reagent with α-ketoacids for the construction of 5-CF3-1,3,4-oxadiazoles that are of importance in medicinal chemistry. The reaction proceeds smoothly witho
Autor:
Yang Huang, Liang Zhao, Qi-Ping Huang, Yanbo Yu, Jia Jia, Jiwei Gu, Jie Tong, An-Jun Wang, Chun-Yang He
Publikováno v:
Organic Chemistry Frontiers. 8:4438-4444
Hantzsch ester, a widely used base or electron-donor compound, was found to act as a catalyst in the deaminative difluoroalkylation reaction utilizing Katritzky salts and difluoroenoxysilane as substrates; this represents a rare catalytic example of
Publikováno v:
Organic Chemistry Frontiers. 8:5322-5327
Iron-catalyzed functionalization of inert bonds has scarcely been documented. Herein, we report an iron-catalyzed method for the silylation and borylation of (hetero)aromatic fluorides. This protocol features a wide range of substrates, high efficien
Publikováno v:
Advanced Synthesis & Catalysis. 362:2604-2608
Publikováno v:
Organic Letters. 22:2816-2821
To date, the iron-catalyzed construction of C–heteroatom bonds has been less developed due to the difficulty of transmetalation with heteroatom anions and the sluggish reductive elimination. Herein...