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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Microwave-assisted transamidation of ureas von Wang, Tammy C., Qiao, Jennifer X.

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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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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 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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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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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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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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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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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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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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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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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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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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Potent P2Y1 urea antagonists bearing various cyclic amine scaffolds von Ruel, Réjean, L’Heureux, Alexandre, Thibeault, Carl, Lapointe, Philippe, Martel, Alain, Qiao, Jennifer X., Hua, Ji, Price, Laura A., Wu, Qimin, Chang, Ming, Zheng, Joanna, Huang, Christine S., Wexler, Ruth R., Rehfuss, Robert, Lam, Patrick Y.S.

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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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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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