Efficient Synthesis of Spirooxindole Pyrrolones by a Rhodium(III)‐Catalyzed C−H Activation/Carbene Insertion/Lossen Rearrangement Sequence von Ma, Biao, Wu, Peng, Wang, Xing, Wang, Zhengyu, Lin, Hai‐Xia, Dai, Hui‐Xiong

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C−X (X=C, O, S, N, B, P) Bond Deuteration and Late‐Stage Applications von Xu, Hui, Zhang, Yun‐Qian, Dai, Hui‐Xiong

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Pd(II)-Catalyzed ortho- or meta-C–H Olefination of Phenol Derivatives von Dai, Hui-Xiong, Li, Gang, Zhang, Xing-Guo, Stepan, Antonia F, Yu, Jin-Quan

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Overcoming the limitations of directed C–H functionalizations of heterocycles von Liu, Yue-Jin, Xu, Hui, Kong, Wei-Jun, Shang, Ming, Dai, Hui-Xiong, Yu, Jin-Quan

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Pd-Catalyzed Oxidative ortho-C–H Borylation of Arenes von Dai, Hui-Xiong, Yu, Jin-Quan

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Pd(II)-Catalyzed Hydroxyl-Directed C−H Activation/C−O Cyclization: Expedient Construction of Dihydrobenzofurans von Wang, Xisheng, Lu, Yi, Dai, Hui-Xiong, Yu, Jin-Quan

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Transformations of Aryl Ketones via Ligand‐Promoted C−C Bond Activation von Li, Hanyuan, Ma, Biao, Liu, Qi‐Sheng, Wang, Mei‐Ling, Wang, Zhen‐Yu, Xu, Hui, Li, Ling‐Jun, Wang, Xing, Dai, Hui‐Xiong

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Palladium‐Catalyzed Deuteration of Arylketone Oxime Ethers von Wang, Zhen‐Yu, Zhang, Xu, Chen, Wen‐Qing, Sun, Guo‐Dong, Wang, Xing, Tan, Lin, Xu, Hui, Dai, Hui‐Xiong

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Copper‐Mediated Late‐Stage Functionalization of Heterocycle‐Containing Molecules von Shang, Ming, Wang, Ming‐Ming, Saint‐Denis, Tyler G., Li, Ming‐Hong, Dai, Hui‐Xiong, Yu, Jin‐Quan

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Divergent C–H Functionalizations Directed by Sulfonamide Pharmacophores: Late-Stage Diversification as a Tool for Drug Discovery von Dai, Hui-Xiong, Stepan, Antonia F, Plummer, Mark S, Zhang, Yang-Hui, Yu, Jin-Quan

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Pd-Catalyzed Asymmetric Dearomatization of Indoles via Decarbonylative Heck-Type Reaction of Thioesters von Han, Ming-Liang, Huang, Wei, Liu, Yu-Wen, Liu, Min, Xu, Hui, Xiong, Hai, Dai, Hui-Xiong

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Construction of polysubstituted pentafulvenes via palladium-catalyzed deacetylation of enones von Li, Ling-Jun, Wang, Xing, Xu, Hui, Dai, Hui-Xiong

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Ligand-enabled ortho -C-H olefination of phenylacetic amides with unactivated alkenes von Lu, Ming-Zhu, Chen, Xing-Rong, Xu, Hui, Dai, Hui-Xiong, Yu, Jin-Quan

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Exceedingly Fast Copper(II)-Promoted ortho CH Trifluoromethylation of Arenes using TMSCF3 von Shang, Ming, Sun, Shang-Zheng, Wang, Hong-Li, Laforteza, Brian N., Dai, Hui-Xiong, Yu, Jin-Quan

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Ru(II)-Catalyzed ortho-C–H Amination of Arenes and Heteroarenes at Room Temperature von Shang, Ming, Zeng, Shao-Hang, Sun, Shang-Zheng, Dai, Hui-Xiong, Yu, Jin-Quan

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Mizoroki–Heck Reaction of Unstrained Aryl Ketones via Ligand-Promoted C–C Bond Olefination von Wang, Mei-Ling, Xu, Hui, Li, Han-Yuan, Ma, Biao, Wang, Zhen-Yu, Wang, Xing, Dai, Hui-Xiong

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Ligand-Promoted Borylation of C(sp3)H Bonds with Palladium(II) Catalysts von He, Jian, Jiang, Heng, Takise, Ryosuke, Zhu, Ru-Yi, Chen, Gang, Dai, Hui-Xiong, Dhar, T. G. Murali, Shi, Jun, Zhang, Hao, Cheng, Peter T. W., Yu, Jin-Quan

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Total Synthesis of Syringin and Its Natural Analogues via C—C Bond Activation of Aryl Ketones von Wang, Zhen‐Yu, Sun, Yi, Sun, Guo‐Dong, Xu, Hui, Dai, Hui‐Xiong

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Construction of 2-alkynyl aza-spiro[4,5]indole scaffolds via sequential C–H activations for modular click chemistry libraries von Zhang, Jun, Wang, Mengmeng, Wang, Huiying, Xu, Hui, Chen, Junjie, Guo, Ziqiong, Ma, Biao, Ban, Shu-Rong, Dai, Hui-Xiong

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Ligand-Promoted Alkynylation of Aryl Ketones: A Practical Tool for Structural Diversity in Drugs and Natural Products von Xu, Hui, Ma, Biao, Fu, Zunyun, Li, Han-Yuan, Wang, Xing, Wang, Zhen-Yu, Li, Ling-Jun, Cheng, Tai-Jin, Zheng, Mingyue, Dai, Hui-Xiong

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