Search Results - "Yao, Wubing"

Sodium Triethylborohydride-Catalyzed Controlled Reduction of Unactivated Amides to Secondary or Tertiary Amines by Yao, Wubing, He, Lili, Han, Deman, Zhong, Aiguo

“…The first transition-metal-free catalytic protocol for controlled reduction of amide functions using cheap and bench-stable hydrosilanes as reducing agents has…”
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Selective Catalytic Transfer Dehydrogenation of Alkanes and Heterocycles by an Iridium Pincer Complex by Yao, Wubing, Zhang, Yuxuan, Jia, Xiangqing, Huang, Zheng

“…Catalytic alkane dehydrogenation is a reaction with tremendous potential for application. We describe a highly active PSCOP‐pincer iridium catalyst for…”
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Combined KOH/BEt3 Catalyst for Selective Deaminative Hydroboration of Aromatic Carboxamides for Construction of Luminophores by Yao, Wubing, Wang, Jiali, Zhong, Aiguo, Li, Jinshan, Yang, Jianguo

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An Additive-Free, Base-Catalyzed Protodesilylation of Organosilanes by Yao, Wubing, Li, Rongrong, Jiang, Huajiang, Han, Deman

“…We report an additive-free, base-catalyzed C–, N–, O–, and S–Si bond cleavage of various organosilanes in mild conditions. The novel catalyst system exhibits…”
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A Pincer Ruthenium Complex for Regioselective C–H Silylation of Heteroarenes by Fang, Huaquan, Guo, Le, Zhang, Yuxuan, Yao, Wubing, Huang, Zheng

“…A pincer Ru­(II) catalyst for the highly efficient undirected silylation of O- and S-heteroarenes with (TMSO)2MeSiH and Et3SiH is described, producing…”
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Ru‐Catalyzed Selective C(sp3)−H Monoborylation of Amides and Esters by Yao, Wubing, Yang, Jianguo, Hao, Feiyue

“…A ruthenium‐catalyzed method has been developed for the C(sp3)−H monoborylation of various unactivated alkyl and aryl amides and challenging esters, with a…”
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Synthesis of Pincer Hydrido Ruthenium Olefin Complexes for Catalytic Alkane Dehydrogenation by Zhang, Yuxuan, Fang, Huaquan, Yao, Wubing, Leng, Xuebing, Huang, Zheng

“…A series of new hydrido Ru­(II) olefin complexes supported by isopropyl-substituted pincer ligands have been synthesized and characterized. These complexes are…”
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Environmentally Benign, Base-Promoted Selective Amination of Polyhalogenated Pyridines by Sun, Chao, Yao, Wubing, Chen, Xu, Zhao, Yiwen, Wei, Qiqi, Chen, Zishuang, Wu, Jiashou, Hao, Feiyue, Xie, Huiping

“…An environmentally benign, highly efficient, and base-promoted selective amination of various polyhalogenated pyridines including the challenging pyridine…”
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Selective Catalytic Transfer Dehydrogenation of Alkanes and Heterocycles by an Iridium Pincer Complex by Yao, Wubing, Zhang, Yuxuan, Jia, Xiangqing, Huang, Zheng

“…Catalytic alkane dehydrogenation is a reaction with tremendous potential for application. We describe a highly active PSCOP‐pincer iridium catalyst for…”
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Selective hydrogenation of the C C bond in cinnamaldehyde over an ultra-small Pd-Ag alloy catalyst by Li, Rongrong, Yao, Wubing, Jin, Yanxian, Jia, Wenping, Chen, Xiaoying, Chen, Jingjing, Zheng, Jianli, Hu, Yuan, Han, Deman, Zhao, Jia

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Iridium-Catalyzed Selective α‑Alkylation of Unactivated Amides with Primary Alcohols by Guo, Le, Liu, Yinghua, Yao, Wubing, Leng, Xuebing, Huang, Zheng

“…The first α-alkylation of unactivated amides with primary alcohols is described. An effective and robust iridium pincer complex has been developed for…”
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A BEt3‑Base Catalyst for Amide Reduction with Silane by Yao, Wubing, Fang, Huaquan, He, Qiaoxing, Peng, Dongjie, Liu, Guixia, Huang, Zheng

“…Reported herein is the development of a simple but practical catalytic system for the selective reduction of amides with hydrosilane or hydrosiloxane. Low-cost…”
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Ru-Catalyzed ortho-Selective Diborylation of 2‑Arylpyridines toward the Construction of π‑Conjugated Functions by Yao, Wubing, Wang, Jiali, He, Lili, Cao, Dongdong, Yang, Jianguo

“…A ruthenium catalytic ortho-C–H diborylation of 2-arylpyridine derivatives, including challenging 2-phenoxypyridine functions, using a remarkably low catalyst…”
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Catalytic alkane dehydrogenations by Zhang, Yuxuan, Yao, Wubing, Fang, Huaquan, Hu, Aiguo, Huang, Zheng

“…Olefins find widespread applications in the synthesis of polyolefins and fine chemicals. With an increasing demand for olefins, the technologies for alkane…”
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Combined KOH/BEt 3 Catalyst for Selective Deaminative Hydroboration of Aromatic Carboxamides for Construction of Luminophores by Yao, Wubing, Wang, Jiali, Zhong, Aiguo, Li, Jinshan, Yang, Jianguo

“…The selective catalytic C-N bond cleavage of amides into value-added amine products is a desirable but challenging transformation. Molecules containing…”
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Cobalt-Catalyzed Borylation of Aryl Halides and Pseudohalides by Yao, Wubing, Fang, Huaquan, Peng, Sihan, Wen, Huanan, Zhang, Lei, Hu, Aiguo, Huang, Zheng

“…We report the first Co-catalyzed borylation of aryl halides and pseudohalides with bis­(pinacolato)­diboron (B2pin2). The synthesis of two new Co­(II)…”
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Catalyst‐ and Additive‐Free Chemoselective Transfer Hydrogenation of α‐Keto Amides to α‐Hydroxy Amides by Sodium Formate by Hao, Feiyue, Gu, Zhenyu, Liu, Guyue, Yao, Wubing, Jiang, Huajiang, Wu, Jiashou

“…A catalyst‐ and additive‐free chemoselective transfer hydrogenation of α‐keto amides to α‐hydroxy amides is easily achieved by using sodium formate as a…”
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Dissolution behaviour and thermodynamic properties of rubidate in (methanol + water) and (ethanol + water) mixtures from T=(278.15 to 318.15) K by Li, Rongrong, Yao, Wubing, Zhang, Bin, Chen, Di, Wang, Fang, Zhu, Chunyan, Wang, Wei, Chen, Xianlang, Xu, Qianqian, Han, Deman

“…[Display omitted] Due to the poor water solubility of rubidate, it is difficult to prepare and apply. In this work, the objective is to study the dissolution…”
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Catalytic alkane transfer-dehydrogenation by PSCOP iridium pincer complexes by Yao, Wubing, Jia, Xiangqing, Leng, Xuebing, Goldman, Alan S., Brookhart, Maurice, Huang, Zheng

“…New (tBu2PSCOPR2)IrHCl iridium complexes ligated by hybrid phosphinothious-phosphinite PSCOP ligands have been synthesized and characterized. The steric…”
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A highly efficient catalytic α-alkylation of unactivated amides using primary alcohols by Yao, Wubing, Ma, Xiaochen, Guo, Le, Jia, Xiangqing, Hu, Aiguo, Huang, Zheng

“…[Display omitted] •Unprecedented high activity for α-alkylations of unactivated amides.•Mild reaction conditions and low catalyst loadings.•Broad substrate…”
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