The Jiao Group

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139. Fe-catalyzed Amination of (Hetero)Arenes with a Redox-active Aminating Reagent under Mild Conditions, Jianzhong Liu, Kai Wu, Tao Shen, Yujie Liang, Miancheng Zou, Yuchao Zhu and Ning Jiao*, Chem. Eur. J. 2017, 23(3), 563-567. Link
139. Fe-catalyzed Amination of (Hetero)Arenes with a Redox-active Aminating Reagent under Mild Conditions, Jianzhong Liu, Kai Wu, Tao Shen, Yujie Liang, Miancheng Zou, Yuchao Zhu and Ning Jiao*, Chem. Eur. J. 2017, 23(3), 563-567.
138. Rh-catalyzed aerobic oxidative cyclization of anilines,alkynes, and CO, Xinyao Li, Jun Pan, Hao Wu, Ning Jiao*, Chem. Sci. 2017, 8, online 10.1039/C7SC02181J. Link
138. Rh-catalyzed aerobic oxidative cyclization of anilines,alkynes, and CO, Xinyao Li, Jun Pan, Hao Wu, Ning Jiao*, Chem. Sci. 2017, 8, online 10.1039/C7SC02181J.
137.[Highlights] Copper-catalyzed enantioselective cyanation of benzylic C–H bonds via radical relay. Liang, Yujie and Jiao, NingScience China Chemistry 60, 105-106 (2016)10.1007/s11426-016-0441-6). Link
137.[Highlights] Copper-catalyzed enantioselective cyanation of benzylic C–H bonds via radical relay. Liang, Yujie and Jiao, NingScience China Chemistry 60, 105-106 (2016)10.1007/s11426-016-0441-6).
136. Direct Tryptophols Synthesis from 2-Vinylanilines and Alkynes via C≡C Triple Bond Cleavage and Dioxygen Activation, Tao Shen, Yiqun Zhang, Yu-Feng Liang, Ning Jiao*, J. Am. Chem. Soc. 2016, 138 (40), 13147-13150. Link
136. Direct Tryptophols Synthesis from 2-Vinylanilines and Alkynes via C≡C Triple Bond Cleavage and Dioxygen Activation, Tao Shen, Yiqun Zhang, Yu-Feng Liang, Ning Jiao*, J. Am. Chem. Soc. 2016, 138 (40), 13147-13150.
135. Dioxygen Promoted Pd-Catalyzed Aminocarbonylation of Organoboronic Acids with Amines and CO: A Direct Approach to Tertiary Amides, Long Ren, Xinwei Li, and Ning Jiao*, Org. Lett. 2016, 18, 5852-5855. Link
135. Dioxygen Promoted Pd-Catalyzed Aminocarbonylation of Organoboronic Acids with Amines and CO: A Direct Approach to Tertiary Amides, Long Ren, Xinwei Li, and Ning Jiao*, Org. Lett. 2016, 18, 5852-5855.
134. Silver-catalyzed Radical Transformation of Aliphatic Carboxylic Acids to Oxime Ethers, Yuchao Zhu, Xiaojin Wen, Song Song,* and Ning Jiao*, Acs. Catal. 2016, 6, 6465–6472. Link
134. Silver-catalyzed Radical Transformation of Aliphatic Carboxylic Acids to Oxime Ethers, Yuchao Zhu, Xiaojin Wen, Song Song,* and Ning Jiao*, Acs. Catal. 2016, 6, 6465–6472.
110. Splitting a Substrate into Three Parts: Gold-Catalyzed Nitrogenation of Alkynes by C-C and C≡C Bond Cleavage, Chong Qin1, Xiaodong Shi* and Ning Jiao*, Angew. Chem. Int. Ed., 55: 350–354. doi: 10.1002/anie.201508347 Link
110. Splitting a Substrate into Three Parts: Gold-Catalyzed Nitrogenation of Alkynes by C-C and C≡C Bond Cleavage, Chong Qin1, Xiaodong Shi* and Ning Jiao*, Angew. Chem. Int. Ed., 55: 350–354. doi: 10.1002/anie.201508347
109. NHPI and palladium cocatalyzed aerobic oxidative acylation of arenes through a radical process, Yu-Feng Liang, Xiaoyang Wang and Ning Jiao*, Chem. Commun., 2016,52, 1416-1419, 10.1039/C5CC08945J Link
109. NHPI and palladium cocatalyzed aerobic oxidative acylation of arenes through a radical process, Yu-Feng Liang, Xiaoyang Wang and Ning Jiao*, Chem. Commun., 2016,52, 1416-1419, 10.1039/C5CC08945J
108. A highly efficient metal-free approach to meta- and multiple-substituted phenols via a simple oxidation of cyclohexenones, Green Chem., 2016,18, 6462-6467, 10.1039/C6GC02674E Link
108. A highly efficient metal-free approach to meta- and multiple-substituted phenols via a simple oxidation of cyclohexenones, Green Chem., 2016,18, 6462-6467, 10.1039/C6GC02674E
107. Conversion of Simple Cyclohexanones into Catechols, Yu-Feng Liang, Xinyao Li and Ning Jiao*, J. Am. Chem. Soc., 2016, 138 (37), pp 12271–12277, DOI: 10.1021/jacs.6b07269 Link
107. Conversion of Simple Cyclohexanones into Catechols, Yu-Feng Liang, Xinyao Li and Ning Jiao*, J. Am. Chem. Soc., 2016, 138 (37), pp 12271–12277, DOI: 10.1021/jacs.6b07269
106. Pd-catalyzed dehydrogenative annulation approach for the efficient synthesis of phenanthridinones, Xinyao Li, Jun Pan, Song Song and Ning Jiao*, Chem. Sci., 2016,7, 5384-5389 , doi: 10.1039/C6SC01148A Link
106. Pd-catalyzed dehydrogenative annulation approach for the efficient synthesis of phenanthridinones, Xinyao Li, Jun Pan, Song Song and Ning Jiao*, Chem. Sci., 2016,7, 5384-5389 , doi: 10.1039/C6SC01148A
105. Coinage metals in organic synthesis, Antonio M. Echavarren, Ning Jiao and Vladimir Gevorgyand, Chem. Soc. Rev., 2016,45, 4445-4447, doi: 10.1039/C6CS90072K Link
105. Coinage metals in organic synthesis, Antonio M. Echavarren, Ning Jiao and Vladimir Gevorgyand, Chem. Soc. Rev., 2016,45, 4445-4447, doi: 10.1039/C6CS90072K
104. Cationic Cobalt(III) Catalyzed Indole Synthesis: The Regioselective Intermolecular Cyclization of N-Nitrosoanilines and Alkynes, Yujie Liang and Ning Jiao*, Angew. Chem. Int. Ed. 2016, 55, 4035. DOI: 10.1002/anie.201511002 Link
104. Cationic Cobalt(III) Catalyzed Indole Synthesis: The Regioselective Intermolecular Cyclization of N-Nitrosoanilines and Alkynes, Yujie Liang and Ning Jiao*, Angew. Chem. Int. Ed. 2016, 55, 4035. DOI: 10.1002/anie.201511002
103. Silver-Catalyzed Decarboxylative Azidation of Aliphatic Carboxylic Acids, Yuchao Zhu, Song Song*, and Ning Jiao*, Org. Lett., 2015, 17 (19), pp 4702–4705, DOI: 10.1021/acs.orglett.5b02155 Link
103. Silver-Catalyzed Decarboxylative Azidation of Aliphatic Carboxylic Acids, Yuchao Zhu, Song Song*, and Ning Jiao*, Org. Lett., 2015, 17 (19), pp 4702–4705, DOI: 10.1021/acs.orglett.5b02155
102. Copper-Catalyzed Aerobic Oxidative C–C Bond Cleavage of Unstrained Ketones with Air and Amines, Wang Zhou*, Wenyou Fan and Ning Jiao*, Org. Lett., 2015, 17 (10), pp 2542–2545, DOI: 10.1021/acs.orglett.5b01114 Link
102. Copper-Catalyzed Aerobic Oxidative C–C Bond Cleavage of Unstrained Ketones with Air and Amines, Wang Zhou*, Wenyou Fan and Ning Jiao*, Org. Lett., 2015, 17 (10), pp 2542–2545, DOI: 10.1021/acs.orglett.5b01114
101. Metal-Free Nitrogenation of 2-Acetylbiphenyls: Expeditious Synthesis of Phenanthridines, Conghui Tang, Yizhi Yuan, and Ning Jiao*, Org. Lett., 2015, 17 (9), pp 2206–2209, DOI: 10.1021/acs.orglett.5b00797 Link
101. Metal-Free Nitrogenation of 2-Acetylbiphenyls: Expeditious Synthesis of Phenanthridines, Conghui Tang, Yizhi Yuan, and Ning Jiao*, Org. Lett., 2015, 17 (9), pp 2206–2209, DOI: 10.1021/acs.orglett.5b00797
100. Mn-Catalyzed Highly Efficient Aerobic Oxidative Hydroxyazidation of Olefins: A Direct Approach to β-Azido Alcohols, Xiang Sun, Xinyao Li and Ning Jiao*, J. Am. Chem. Soc., 2015, 137 (18), pp 6059–6066, DOI: 10.1021/jacs.5b02347 Link
100. Mn-Catalyzed Highly Efficient Aerobic Oxidative Hydroxyazidation of Olefins: A Direct Approach to β-Azido Alcohols, Xiang Sun, Xinyao Li and Ning Jiao*, J. Am. Chem. Soc., 2015, 137 (18), pp 6059–6066, DOI: 10.1021/jacs.5b02347
99. Efficient and Practical Oxidative Bromination and Iodination of Arenes and Heteroarenes with DMSO and Hydrogen Halide: A Mild Protocol for Late-Stage Functionalization,Song Song and Ning Jiao*, Org. Lett., 2015, 17 (12), pp 2886–2889 Link
99. Efficient and Practical Oxidative Bromination and Iodination of Arenes and Heteroarenes with DMSO and Hydrogen Halide: A Mild Protocol for Late-Stage Functionalization,Song Song and Ning Jiao*, Org. Lett., 2015, 17 (12), pp 2886–2889
98. Efficient bromination of olefins, alkynes, and ketones with dimethyl sulfoxide and hydrobromic acid, Song Song, Xinwei Li, Xiang Sun and Ning Jiao*, Green Chem., 2015, 17, Link
98. Efficient bromination of olefins, alkynes, and ketones with dimethyl sulfoxide and hydrobromic acid, Song Song, Xinwei Li, Xiang Sun and Ning Jiao*, Green Chem., 2015, 17,
97. From simple organobromides or olefins to highly value-added bromohydrins: a versatile performance of dimethyl sulfoxide, Song Song, Xiaoqiang Huang and Ning Jiao*, Green Chem., 2015, 17, 2727, DOI: 10.1039/c5gc00184f Link
97. From simple organobromides or olefins to highly value-added bromohydrins: a versatile performance of dimethyl sulfoxide, Song Song, Xiaoqiang Huang and Ning Jiao*, Green Chem., 2015, 17, 2727, DOI: 10.1039/c5gc00184f
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