The Jiao Group

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96. Synergistic Gold and Iron Dual Catalysis: Preferred Radical Addition toward Vinyl–Gold Intermediate over Alkene, Haihui Peng, Ning Jiao*, and Xiaodong Shi*, J. Am. Chem. Soc., 2015, 137 (28), pp 8912–8915, DOI: 10.1021/jacs.5b05415 Link
96. Synergistic Gold and Iron Dual Catalysis: Preferred Radical Addition toward Vinyl–Gold Intermediate over Alkene, Haihui Peng, Ning Jiao*, and Xiaodong Shi*, J. Am. Chem. Soc., 2015, 137 (28), pp 8912–8915, DOI: 10.1021/jacs.5b05415
95. An Iron-Catalyzed Direct Approach to Amides from Benzyl Azides via C–C Bond Cleavage, Yang Ou, Chong Qi and Ning Jiao*, Synthesis 2015, 47, 2971, DOI: 10.1055/s-0034-1380222 Link
95. An Iron-Catalyzed Direct Approach to Amides from Benzyl Azides via C–C Bond Cleavage, Yang Ou, Chong Qi and Ning Jiao*, Synthesis 2015, 47, 2971, DOI: 10.1055/s-0034-1380222
94. I2- or NBS-Catalyzed Highly Efficient α-Hydroxylation of Ketones with Dimethyl Sulfoxide, Yu-Feng Liang, Kai Wu and Ning Jiao*, Org. Lett., 2015, 17 (4), pp 876–879, DOI: 10.1021/ol5037387 Link
94. I2- or NBS-Catalyzed Highly Efficient α-Hydroxylation of Ketones with Dimethyl Sulfoxide, Yu-Feng Liang, Kai Wu and Ning Jiao*, Org. Lett., 2015, 17 (4), pp 876–879, DOI: 10.1021/ol5037387
93. CsOH catalyzed aerobic oxidative synthesis of p-quinols from multi-alkyl phenols under mild conditions, Yu-Feng Liang, Kai Wu and Ning Jiao. China Chem. (2015) 58: 1334. DOI: 10.1007/s11426-015-5363-4 Link
93. CsOH catalyzed aerobic oxidative synthesis of p-quinols from multi-alkyl phenols under mild conditions, Yu-Feng Liang, Kai Wu and Ning Jiao. China Chem. (2015) 58: 1334. DOI: 10.1007/s11426-015-5363-4
92. Ligand-Promoted Pd-Catalyzed Oxime Ether Directed C–H Hydroxylation of Arenes, Yu-Feng Liang, Xiaoyang Wang and Ning Jiao*, ACS Catal., 2015, 5 (10), pp 6148–6152, DOI: 10.1021/acscatal.5b01700 Link
92. Ligand-Promoted Pd-Catalyzed Oxime Ether Directed C–H Hydroxylation of Arenes, Yu-Feng Liang, Xiaoyang Wang and Ning Jiao*, ACS Catal., 2015, 5 (10), pp 6148–6152, DOI: 10.1021/acscatal.5b01700
91. Aerobic Oxidation of PdII to PdIV by Active Radical Reactants: Direct C–H Nitration and Acylation of Arenes via Oxygenation Process with Molecular Oxygen, Yu-Feng Liang, Xinyao Li and Ning Jiao*, ACS Catal., 2015, 5 (3), pp 1956–1963 Link
91. Aerobic Oxidation of PdII to PdIV by Active Radical Reactants: Direct C–H Nitration and Acylation of Arenes via Oxygenation Process with Molecular Oxygen, Yu-Feng Liang, Xinyao Li and Ning Jiao*, ACS Catal., 2015, 5 (3), pp 1956–1963
90. Cu-Catalyzed Concise Synthesis of Pyridines and 2-(1H)-Pyridones from Acetaldehydes and Simple Nitrogen Donors, Ziyuan Li, Xiaoqiang Huang and Ning Jiao*, Org. Lett., 2015, 17 (3), pp 584–587, DOI: 10.1021/ol5035996 Link
90. Cu-Catalyzed Concise Synthesis of Pyridines and 2-(1H)-Pyridones from Acetaldehydes and Simple Nitrogen Donors, Ziyuan Li, Xiaoqiang Huang and Ning Jiao*, Org. Lett., 2015, 17 (3), pp 584–587, DOI: 10.1021/ol5035996
89. Rh-Catalyzed Construction of Quinolin-2(1H)-ones via C–H Bond Activation of Simple Anilines with CO and Alkynes, Xinyao Li, Xinwei Li, and Ning Jiao*, J. Am. Chem. Soc., 2015, 137 (29), pp 9246–9249, DOI: 10.1021/jacs.5b05843 Link
89. Rh-Catalyzed Construction of Quinolin-2(1H)-ones via C–H Bond Activation of Simple Anilines with CO and Alkynes, Xinyao Li, Xinwei Li, and Ning Jiao*, J. Am. Chem. Soc., 2015, 137 (29), pp 9246–9249, DOI: 10.1021/jacs.5b05843
88. TEMP and copper cocatalyzed oxygenation of ketones with molecular oxygen: chemoselective synthesis of α-ketoesters, Xiaoqiang Huang, Xinwei Li, Miancheng Zou and Ning Jiao*, Org. Chem. Front., 2015, 2, 354, DOI: 10.1039/c5qo00028a Link
88. TEMP and copper cocatalyzed oxygenation of ketones with molecular oxygen: chemoselective synthesis of α-ketoesters, Xiaoqiang Huang, Xinwei Li, Miancheng Zou and Ning Jiao*, Org. Chem. Front., 2015, 2, 354, DOI: 10.1039/c5qo00028a
87. NBS mediated nitriles synthesis through C[double bond, length as m-dash]C double bond cleavage, Xiaolin Zong,a Qing-Zhong Zhenga and Ning Jiao*, Org. Biomol. Chem., 2014, 12, 1198, DOI: 10.1039/c3ob42118j Link
87. NBS mediated nitriles synthesis through C[double bond, length as m-dash]C double bond cleavage, Xiaolin Zong,a Qing-Zhong Zhenga and Ning Jiao*, Org. Biomol. Chem., 2014, 12, 1198, DOI: 10.1039/c3ob42118j
86. Transition-metal-catalyzed ketone-directed ortho-C–H functionalization reactions Link
86. Transition-metal-catalyzed ketone-directed ortho-C–H functionalization reactions
85. Copper-Catalyzed Aerobic Oxidative C–C Bond Cleavage of 1,3-Diaryl­diketones To Synthesize 1,2-Diketones, Chun Zhang, Xiaoyang Wang, Ning Jiao*, Synlett 2014; 25(10): 1458-1460, DOI: 10.1055/s-0033-1341243 Link
85. Copper-Catalyzed Aerobic Oxidative C–C Bond Cleavage of 1,3-Diaryl­diketones To Synthesize 1,2-Diketones, Chun Zhang, Xiaoyang Wang, Ning Jiao*, Synlett 2014; 25(10): 1458-1460, DOI: 10.1055/s-0033-1341243
84. Copper-Catalyzed Oxoazidation and Alkoxyazidation of Indoles, Hang Yin, Teng Wang, and Ning Jiao*, Org. Lett., 2014, 16 (9), pp 2302–2305, DOI: 10.1021/ol500793c Link
84. Copper-Catalyzed Oxoazidation and Alkoxyazidation of Indoles, Hang Yin, Teng Wang, and Ning Jiao*, Org. Lett., 2014, 16 (9), pp 2302–2305, DOI: 10.1021/ol500793c
83. Direct Approaches to Nitriles via Highly Efficient Nitrogenation Strategy through C–H or C–C Bond Cleavage, Teng Wang and Ning Jiao*, Acc. Chem. Res., 2014, 47 (4), pp 1137–1145, DOI: 10.1021/ar400259e Link
83. Direct Approaches to Nitriles via Highly Efficient Nitrogenation Strategy through C–H or C–C Bond Cleavage, Teng Wang and Ning Jiao*, Acc. Chem. Res., 2014, 47 (4), pp 1137–1145, DOI: 10.1021/ar400259e
82. Copper-Catalyzed Aerobic Oxidative C[BOND]C Bond Cleavage for C[BOND]N Bond Formation: From Ketones to Amides, Conghui Tang and Ning Jiao*, Angew. Chem. Int. Ed., 53: 6528, doi: 10.1002/anie.201403528 Link
82. Copper-Catalyzed Aerobic Oxidative C[BOND]C Bond Cleavage for C[BOND]N Bond Formation: From Ketones to Amides, Conghui Tang and Ning Jiao*, Angew. Chem. Int. Ed., 53: 6528, doi: 10.1002/anie.201403528
81. The direct C–H halogenations of indoles, Leilei Shi, Dongmei Zhang and Ning Jiao*, Tetrahedron Letters 55 (2014) 2243, doi: 10.1016/j.tetlet.2014.02.071 Link
81. The direct C–H halogenations of indoles, Leilei Shi, Dongmei Zhang and Ning Jiao*, Tetrahedron Letters 55 (2014) 2243, doi: 10.1016/j.tetlet.2014.02.071
80. Iron-catalyzed aerobic difunctionalization of alkenes: a highly efficient approach to construct oxindoles by C–S and C–C bond formation, Tao Shen, Yizhi Yuan, Song Song and Ning Jiao*, Chem. Commun., 2014, 50, 4115 Link
80. Iron-catalyzed aerobic difunctionalization of alkenes: a highly efficient approach to construct oxindoles by C–S and C–C bond formation, Tao Shen, Yizhi Yuan, Song Song and Ning Jiao*, Chem. Commun., 2014, 50, 4115
79. Metal-free nitro-carbocyclization of activated alkenes: a direct approach to synthesize oxindoles by cascade C–N and C–C bond formation Tao Shen,a Yizhi Yuana and Ning Jiao*, Chem. Commun., 2014, 50, 554, DOI: 10.1039/c3cc47336h Link
79. Metal-free nitro-carbocyclization of activated alkenes: a direct approach to synthesize oxindoles by cascade C–N and C–C bond formation Tao Shen,a Yizhi Yuana and Ning Jiao*, Chem. Commun., 2014, 50, 554, DOI: 10.1039/c3cc47336h
78. PdCl2 catalyzed efficient assembly of organic azides, CO, and alcohols under mild conditions: a direct approach to synthesize carbamates Long Rena and Ning Jiao*, Chem. Commun., 2014, 50, 3706, doi:10.1039/C4CC00538D Link
78. PdCl2 catalyzed efficient assembly of organic azides, CO, and alcohols under mild conditions: a direct approach to synthesize carbamates Long Rena and Ning Jiao*, Chem. Commun., 2014, 50, 3706, doi:10.1039/C4CC00538D
77. Pd/Cu-Cocatalyzed Aerobic Oxidative Carbonylative Homocoupling of Arylboronic Acids and CO: A Highly Selective Approach to Diaryl Ketones, Long Ren and Prof. Ning Jiao*, Chem. Asian J., 9: 2411, 10.1002/asia.201402326 Link
77. Pd/Cu-Cocatalyzed Aerobic Oxidative Carbonylative Homocoupling of Arylboronic Acids and CO: A Highly Selective Approach to Diaryl Ketones, Long Ren and Prof. Ning Jiao*, Chem. Asian J., 9: 2411, 10.1002/asia.201402326
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