The Jiao Group

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56. Recyclable copper catalyzed nitrogenation of biphenyl halides: a direct approach to carbazoles, Yang Ou and Ning Jiao*, Chem. Commun., 2013, 49, 3473, DOI: 10.1039/c3cc41443d Link
56. Recyclable copper catalyzed nitrogenation of biphenyl halides: a direct approach to carbazoles, Yang Ou and Ning Jiao*, Chem. Commun., 2013, 49, 3473, DOI: 10.1039/c3cc41443d
55. Copper-catalyzed direct oxidative annulation of N-iminopyridinium ylides with terminal alkynes using O2 as oxidant， Shengtao Ding and Ning Jiao*, Chem. Commun., 2013, 49, 4250, DOI: 10.1039/c2cc33706a Link
55. Copper-catalyzed direct oxidative annulation of N-iminopyridinium ylides with terminal alkynes using O2 as oxidant， Shengtao Ding and Ning Jiao*, Chem. Commun., 2013, 49, 4250, DOI: 10.1039/c2cc33706a
54. Direct Transformation of Methyl Imines to α-Iminonitriles under Mild and Transition-Metal-Free Conditions, Feng Chen and Ning Jiao*, Chem. Eur. J. 2013, 19, 11199, DOI : 10.1002/chem.201301933 Link
54. Direct Transformation of Methyl Imines to α-Iminonitriles under Mild and Transition-Metal-Free Conditions, Feng Chen and Ning Jiao*, Chem. Eur. J. 2013, 19, 11199, DOI : 10.1002/chem.201301933
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
48. Recent advances in copper-catalyzed dehydrogenative functionalization via a single electron transfer (SET) process, Chun Zhang, Conghui Tang and Ning Jiao*, Chem. Soc. Rev., 2012, 41, 3464, DOI: 10.1039/c2cs15323h Link
48. Recent advances in copper-catalyzed dehydrogenative functionalization via a single electron transfer (SET) process, Chun Zhang, Conghui Tang and Ning Jiao*, Chem. Soc. Rev., 2012, 41, 3464, DOI: 10.1039/c2cs15323h
47. N-Heterocyclic Carbene-Catalyzed Homoenolate Additions with N-Aryl Ketimines as Electrophiles: Efficient Synthesis of Spirocyclic g-Lactam Oxindoles, Bo Zhang, Song Ye,* and Ning Jiao*, Chem. Eur. J. 2012, 18, 9198 Link
47. N-Heterocyclic Carbene-Catalyzed Homoenolate Additions with N-Aryl Ketimines as Electrophiles: Efficient Synthesis of Spirocyclic g-Lactam Oxindoles, Bo Zhang, Song Ye,* and Ning Jiao*, Chem. Eur. J. 2012, 18, 9198
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
45. Metal-free TEMPO-catalyzed oxidative C–C bond formation from Csp3–H bonds using molecular oxygen as the oxidant, Bo Zhang,Yuxin Cui and Ning Jiao*, Chem. Commun., 2012, 48, 4498, DOI: 10.1039/c2cc30684k Link
45. Metal-free TEMPO-catalyzed oxidative C–C bond formation from Csp3–H bonds using molecular oxygen as the oxidant, Bo Zhang,Yuxin Cui and Ning Jiao*, Chem. Commun., 2012, 48, 4498, DOI: 10.1039/c2cc30684k
44. Synthesis of Oxazoles through Copper-Mediated Aerobic Oxidative Dehydrogenative Annulation and Oxygenation of Aldehydes and Amines, Zejun Xu, Chun Zhang, and Ning Jiao*, Angew. Chem. Int. Ed. 2012, 51, 11367 Link
44. Synthesis of Oxazoles through Copper-Mediated Aerobic Oxidative Dehydrogenative Annulation and Oxygenation of Aldehydes and Amines, Zejun Xu, Chun Zhang, and Ning Jiao*, Angew. Chem. Int. Ed. 2012, 51, 11367
43. Csp2–Csp2 bond formation via Lewis acid/ammonium salt cocatalyzed tandem addition and oxidative dehydrogenation strategy: alkenylation of indoles with a,b-unsaturated ketones, Link
43. Csp2–Csp2 bond formation via Lewis acid/ammonium salt cocatalyzed tandem addition and oxidative dehydrogenation strategy: alkenylation of indoles with a,b-unsaturated ketones,
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
40. Recent advances in transition-metal catalyzed reactions using molecular oxygen as the oxidant, Zhuangzhi Shi,Chun Zhang,Conghui Tanga and Ning Jiao, Chem. Soc. Rev., 2012, 41, 3381, DOI: 10.1039/c2cs15224j Link
40. Recent advances in transition-metal catalyzed reactions using molecular oxygen as the oxidant, Zhuangzhi Shi,Chun Zhang,Conghui Tanga and Ning Jiao, Chem. Soc. Rev., 2012, 41, 3381, DOI: 10.1039/c2cs15224j
39. Chemoselective Synthesis of Naphthylamides and Isoquinolinones via Rhodium-Catalyzed Oxidative Dehydrogenative Annulation of Benzamides with Alkynes, Zhuangzhi Shi1, Conghui Tang1, and Ning Jiao*, Adv. Synth. Catal. 2012, 354, 2695 Link
39. Chemoselective Synthesis of Naphthylamides and Isoquinolinones via Rhodium-Catalyzed Oxidative Dehydrogenative Annulation of Benzamides with Alkynes, Zhuangzhi Shi1, Conghui Tang1, and Ning Jiao*, Adv. Synth. Catal. 2012, 354, 2695
38. FeCl2-Promoted Cleavage of the Unactivated CC Bond of Alkylarenes and Polystyrene : Direct Synthesis of Arylamines, Chong Qin and Ning Jiao*, Angew. Chem. Int. Ed. 2012, 51, 6971, DOI : 10.1002/anie.201202464 Link
38. FeCl2-Promoted Cleavage of the Unactivated CC Bond of Alkylarenes and Polystyrene : Direct Synthesis of Arylamines, Chong Qin and Ning Jiao*, Angew. Chem. Int. Ed. 2012, 51, 6971, DOI : 10.1002/anie.201202464
37. Metal-Free, NHPI Catalyzed Oxidative Cleavage of C–C Double Bond Using Molecular Oxygen as Oxidant Link
37. Metal-Free, NHPI Catalyzed Oxidative Cleavage of C–C Double Bond Using Molecular Oxygen as Oxidant
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