The Jiao Group

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53. Copper-Catalyzed Aerobic Oxidative Cross-Dehydrogenative Coupling of Amine and α-Carbonyl Aldehyde: A Practical and Efficient Approach to α-Ketoamides with Wide Substrate Scope, Chun Zhang and Ning Jiao*, Org. Lett., 2012, 14 ,pp 3280 Link
53. Copper-Catalyzed Aerobic Oxidative Cross-Dehydrogenative Coupling of Amine and α-Carbonyl Aldehyde: A Practical and Efficient Approach to α-Ketoamides with Wide Substrate Scope, Chun Zhang and Ning Jiao*, Org. Lett., 2012, 14 ,pp 3280
52. Catalyst free approach to benzimidazoles using air as the oxidant at room temperature, Chun Zhang and Ning Jiao*, Green Chem., 2012, 14, 3273, DOI: 10.1039/c2gc36416f Link
52. Catalyst free approach to benzimidazoles using air as the oxidant at room temperature, Chun Zhang and Ning Jiao*, Green Chem., 2012, 14, 3273, DOI: 10.1039/c2gc36416f
51. Multiple Oxidative Dehydrogenative Functionalization of Arylacetaldehydes Using Molecular Oxygen as Oxidant Leading to 2-Oxo-acetamidines, Chun Zhang,Liangren Zhang and Ning Jiao*, Adv. Synth. Catal. 2012, 354, 1293 Link
51. Multiple Oxidative Dehydrogenative Functionalization of Arylacetaldehydes Using Molecular Oxygen as Oxidant Leading to 2-Oxo-acetamidines, Chun Zhang,Liangren Zhang and Ning Jiao*, Adv. Synth. Catal. 2012, 354, 1293
50. Et3N-catalyzed oxidative dehydrogenative coupling of a-unsubstituted aldehydes and ketones with aryl diamines leading to quinoxalines using molecular oxygen as oxidant, Chun Zhang and Ning Jiao*, Tetrahedron 68 (2012) 5258e5262 Link
50. Et3N-catalyzed oxidative dehydrogenative coupling of a-unsubstituted aldehydes and ketones with aryl diamines leading to quinoxalines using molecular oxygen as oxidant, Chun Zhang and Ning Jiao*, Tetrahedron 68 (2012) 5258e5262
49. Mn-promoted Aerobic Oxidative C–C Bond Cleavage of Aldehydes with Dioxygen Activation: A Simple Synthetic Approach to Formamides, Chun Zhang and Ning Jiao*, Org. Lett., 2012, 14 (9), pp 2362–2365 Link
49. Mn-promoted Aerobic Oxidative C–C Bond Cleavage of Aldehydes with Dioxygen Activation: A Simple Synthetic Approach to Formamides, Chun Zhang and Ning Jiao*, Org. Lett., 2012, 14 (9), pp 2362–2365
46. NHC-catalyzed C–O or C–N bond formation: efficient approaches, Bo Zhang, Peng Feng and Ning Jiao*, Chem. Commun., 2012, 48, 7280, DOI: 10.1039/c2cc32862c Link
46. NHC-catalyzed C–O or C–N bond formation: efficient approaches, Bo Zhang, Peng Feng and Ning Jiao*, Chem. Commun., 2012, 48, 7280, DOI: 10.1039/c2cc32862c
42. Iron-Facilitated Oxidative Dehydrogenative CO Bond Formation by Propargylic Csp3H Functionalization, Teng Wang and Ning Jiao*, Angew. Chem. Int. Ed. 2012, 51, 10823, DOI : 10.1002/anie.201205779 Link
42. Iron-Facilitated Oxidative Dehydrogenative CO Bond Formation by Propargylic Csp3H Functionalization, Teng Wang and Ning Jiao*, Angew. Chem. Int. Ed. 2012, 51, 10823, DOI : 10.1002/anie.201205779
41. Copper-Catalyzed C–H Azidation of Anilines under Mild Conditions, Conghui Tang and Ning Jiao*, J. Am. Chem. Soc., 2012, 134 (46), pp 18924–18927, DOI: 10.1021/ja3089907 Link
41. Copper-Catalyzed C–H Azidation of Anilines under Mild Conditions, Conghui Tang and Ning Jiao*, J. Am. Chem. Soc., 2012, 134 (46), pp 18924–18927, DOI: 10.1021/ja3089907
36. N,N-Dimethylformamide : A Multipurpose Building Block, Shengtao Ding and Ning Jiao*, Angew. Chem. Int. Ed. 2012, 51, 9226, DOI : 10.1002/anie.201200859 Link
36. N,N-Dimethylformamide : A Multipurpose Building Block, Shengtao Ding and Ning Jiao*, Angew. Chem. Int. Ed. 2012, 51, 9226, DOI : 10.1002/anie.201200859
35. 2,4- vs 3,4-Disubsituted Pyrrole Synthesis Switched by Copper and Nickel Catalysts, Feng Chen and Ning Jiao*, Org. Lett., 2012, 14 (18), pp 4926–4929, DOI: 10.1021/ol302270z Link
35. 2,4- vs 3,4-Disubsituted Pyrrole Synthesis Switched by Copper and Nickel Catalysts, Feng Chen and Ning Jiao*, Org. Lett., 2012, 14 (18), pp 4926–4929, DOI: 10.1021/ol302270z