Ligand-controlled divergent dehydrogenative reactions of carboxylic acids via C-H activation von Wang, Zhen, Hu, Liang, Chekshin, Nikita, Zhuang, Zhe, Qian, Shaoqun, Qiao, Jennifer X, Yu, Jin-Quan

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Overcoming the Limitations of γ- and δ‑C–H Arylation of Amines through Ligand Development von Chen, Yan-Qiao, Wang, Zhen, Wu, Yongwei, Wisniewski, Steven R, Qiao, Jennifer X, Ewing, William R, Eastgate, Martin D, Yu, Jin-Quan

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Palladium(II)‐Catalyzed Site‐Selective C(sp3)−H Alkynylation of Oligopeptides: A Linchpin Approach for Oligopeptide–Drug Conjugation von Liu, Tao, Qiao, Jennifer X., Poss, Michael A., Yu, Jin‐Quan

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Ligand-Enabled C–H Hydroxylation with Aqueous H2O2 at Room Temperature von Li, Zhen, Park, Han Seul, Qiao, Jennifer X., Yeung, Kap-Sun, Yu, Jin-Quan

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Decarboxylative alkylation for site-selective bioconjugation of native proteins via oxidation potentials von Bloom, Steven, Liu, Chun, Kölmel, Dominik K., Qiao, Jennifer X., Zhang, Yong, Poss, Michael A., Ewing, William R., MacMillan, David W. C.

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Ligand-accelerated non-directed C–H functionalization of arenes von Wang, Peng, Verma, Pritha, Xia, Guoqin, Shi, Jun, Qiao, Jennifer X., Tao, Shiwei, Cheng, Peter T. W., Poss, Michael A., Farmer, Marcus E., Yeung, Kap-Sun, Yu, Jin-Quan

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Pd-Catalyzed γ-C(sp 3 )-H Fluorination of Free Amines von Chen, Yan-Qiao, Singh, Sukriti, Wu, Yongwei, Wang, Zhen, Hao, Wei, Verma, Pritha, Qiao, Jennifer X, Sunoj, Raghavan B, Yu, Jin-Quan

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Versatile Copper-Catalyzed γ‑C(sp3)–H Lactonization of Aliphatic Acids von Zhuang, Zhe, Sheng, Tao, Qiao, Jennifer X., Yeung, Kap-Sun, Yu, Jin-Quan

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Ligand-Enabled Pd(II)-Catalyzed C(sp3)–H Lactonization Using Molecular Oxygen as Oxidant von Qian, Shaoqun, Li, Zi-Qi, Li, Minyan, Wisniewski, Steven R, Qiao, Jennifer X, Richter, Jeremy M, Ewing, William R, Eastgate, Martin D, Chen, Jason S, Yu, Jin-Quan

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Site-Selective Functionalization of Methionine Residues via Photoredox Catalysis von Kim, Junyong, Li, Beryl X, Huang, Richard Y.-C, Qiao, Jennifer X, Ewing, William R, MacMillan, David W. C

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Pd II -Catalyzed Enantioselective C(sp 3 )-H Activation/Cross-Coupling Reactions of Free Carboxylic Acids von Hu, Liang, Shen, Peng-Xiang, Shao, Qian, Hong, Kai, Qiao, Jennifer X, Yu, Jin-Quan

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Site-selective tyrosine bioconjugation via photoredox catalysis for native-to-bioorthogonal protein transformation von Li, Beryl X., Kim, Daniel K., Bloom, Steven, Huang, Richard Y.-C., Qiao, Jennifer X., Ewing, William R., Oblinsky, Daniel G., Scholes, Gregory D., MacMillan, David W. C.

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Synthesis of 1,3-Dienes via Ligand-Enabled Sequential Dehydrogenation of Aliphatic Acids von Meng, Guangrong, Hu, Liang, Chan, Hau Sun Sam, Qiao, Jennifer X., Yu, Jin-Quan

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A tautomeric ligand enables directed C‒H hydroxylation with molecular oxygen von Li, Zhen, Wang, Zhen, Chekshin, Nikita, Qian, Shaoqun, Qiao, Jennifer X., Cheng, Peter T., Yeung, Kap-Sun, Ewing, William R., Yu, Jin-Quan

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Transient Directing Group Enabled Pd-Catalyzed γ‑C(sp3)–H Oxygenation of Alkyl Amines von Chen, Yan-Qiao, Wu, Yongwei, Wang, Zhen, Qiao, Jennifer X, Yu, Jin-Quan

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meta C–H Arylation of Electron-Rich Arenes: Reversing the Conventional Site Selectivity von Liu, Luo-Yan, Qiao, Jennifer X, Yeung, Kap-Sun, Ewing, William R, Yu, Jin-Quan

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One-Step Synthesis of β‑Alkylidene-γ-lactones via Ligand-Enabled β,γ-Dehydrogenation of Aliphatic Acids von Sheng, Tao, Zhuang, Zhe, Wang, Zhen, Hu, Liang, Herron, Alastair N., Qiao, Jennifer X., Yu, Jin-Quan

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meta‐Selective C−H Arylation of Fluoroarenes and Simple Arenes von Liu, Luo‐Yan, Qiao, Jennifer X., Yeung, Kap‐Sun, Ewing, William R., Yu, Jin‐Quan

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Iridium(I)-Catalyzed α‑C(sp3)–H Alkylation of Saturated Azacycles von Verma, Pritha, Richter, Jeremy M, Chekshin, Nikita, Qiao, Jennifer X, Yu, Jin-Quan

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Decarboxylative Peptide Macrocyclization through Photoredox Catalysis von McCarver, Stefan J., Qiao, Jennifer X., Carpenter, Joseph, Borzilleri, Robert M., Poss, Michael A., Eastgate, Martin D., Miller, Michael M., MacMillan, David W. C.

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