The Jiao Group

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20. Copper-Catalyzed Aerobic Oxidative Dehydrogenative Coupling of Anilines Leading to Aromatic Azo Compounds using Dioxygen as an Oxidant, Chun Zhang and Ning Jiao, Angew. Chem. Int. Ed. 2010, 49, 6174 –6177, DOI: 10.1002/anie.201001651 Link
20. Copper-Catalyzed Aerobic Oxidative Dehydrogenative Coupling of Anilines Leading to Aromatic Azo Compounds using Dioxygen as an Oxidant, Chun Zhang and Ning Jiao, Angew. Chem. Int. Ed. 2010, 49, 6174 –6177, DOI: 10.1002/anie.201001651
19. Dioxygen Activation under Ambient Conditions: Cu-Catalyzed Oxidative Amidation−Diketonization of Terminal Alkynes Leading to α-Ketoamides, Chun Zhang and Ning Jiao*, J. Am. Chem. Soc., 2010, 132 (1), pp 28–29, DOI: 10.1021/ja908911n Link
19. Dioxygen Activation under Ambient Conditions: Cu-Catalyzed Oxidative Amidation−Diketonization of Terminal Alkynes Leading to α-Ketoamides, Chun Zhang and Ning Jiao*, J. Am. Chem. Soc., 2010, 132 (1), pp 28–29, DOI: 10.1021/ja908911n
18. Copper-catalyzed decarboxylative cross-coupling of propiolic acids and terminal alkynes, Miao Yu*, Delin Pan and Ning Jiao*, Tetrahedron Letters 51 (2010) 1287–1290, doi:10.1016/j.tetlet.2009.12.138 Link
18. Copper-catalyzed decarboxylative cross-coupling of propiolic acids and terminal alkynes, Miao Yu*, Delin Pan and Ning Jiao*, Tetrahedron Letters 51 (2010) 1287–1290, doi:10.1016/j.tetlet.2009.12.138
17. Palladium-Catalyzed Ring-Expansion Reaction of Indoles with Alkynes: From Indoles to Tetrahydroquinoline Derivatives Under Mild Reaction Conditions, Zhuangzhi Shi and Ning Jiao, Angew. Chem. Int. Ed. 2010, 49, 4036 Link
17. Palladium-Catalyzed Ring-Expansion Reaction of Indoles with Alkynes: From Indoles to Tetrahydroquinoline Derivatives Under Mild Reaction Conditions, Zhuangzhi Shi and Ning Jiao, Angew. Chem. Int. Ed. 2010, 49, 4036
16. Synthesis of β- and γ-Carbolinones via Pd-Catalyzed Direct Dehydrogenative Annulation (DDA) of Indole-carboxamides with Alkynes Using Air as the Oxidant, Zhuangzhi Shi, Yuxin Cui* and Ning Jiao*, Org. Lett., 2010, 12 (13), pp 2908–2911 Link
16. Synthesis of β- and γ-Carbolinones via Pd-Catalyzed Direct Dehydrogenative Annulation (DDA) of Indole-carboxamides with Alkynes Using Air as the Oxidant, Zhuangzhi Shi, Yuxin Cui* and Ning Jiao*, Org. Lett., 2010, 12 (13), pp 2908–2911
14. PdII-Catalyzed Highly Selective Arylation of Allyl Esters via C-H Functionalization of Unreactive Arenes with Retention of the Traditional Leaving Group, Delin Pan, Miao Yu,* and Ning Jiao*, Chem. Asian J. 2010, 5, 1090 Link
14. PdII-Catalyzed Highly Selective Arylation of Allyl Esters via C-H Functionalization of Unreactive Arenes with Retention of the Traditional Leaving Group, Delin Pan, Miao Yu,* and Ning Jiao*, Chem. Asian J. 2010, 5, 1090
12. Cu-Catalyzed Oxidative Amidation of Propiolic Acids Under Air via Decarboxylative Coupling, Wei Jia and Ning Jiao*, Org. Lett., 2010, 12 (9), pp 2000–2003 DOI: 10.1021/ol1004615 Link
12. Cu-Catalyzed Oxidative Amidation of Propiolic Acids Under Air via Decarboxylative Coupling, Wei Jia and Ning Jiao*, Org. Lett., 2010, 12 (9), pp 2000–2003 DOI: 10.1021/ol1004615
11. Pd(II)-Catalyzed Synthesis of Carbolines by Iminoannulation of Internal Alkynes via Direct C−H Bond Cleavage Using Dioxygen as Oxidant, Shengtao Ding and Ning Jiao*, Org. Lett., 2010, 12 (7), pp 1540–1543. DOI: 10.1021/ol100272s Link
11. Pd(II)-Catalyzed Synthesis of Carbolines by Iminoannulation of Internal Alkynes via Direct C−H Bond Cleavage Using Dioxygen as Oxidant, Shengtao Ding and Ning Jiao*, Org. Lett., 2010, 12 (7), pp 1540–1543. DOI: 10.1021/ol100272s
7. Control of Chemo-, Regio-, and Stereoselectivities in Ligand-Free Pd-Catalyzed Oxidative Heck Reactions of Arylboronic Acids or Alkenylboronate with Allyl Esters,Yijin Su and Ning Jiao, Org. Lett., 2009, 11 (14), pp 2980–2983 Link
7. Control of Chemo-, Regio-, and Stereoselectivities in Ligand-Free Pd-Catalyzed Oxidative Heck Reactions of Arylboronic Acids or Alkenylboronate with Allyl Esters,Yijin Su and Ning Jiao, Org. Lett., 2009, 11 (14), pp 2980–2983
6. Indoles from Simple Anilines and Alkynes : Palladium-Catalyzed C-H Activation Using Dioxygen as the Oxidant, Zhuangzhi Shi and Ning Jiao, Angew. Chem. Int. Ed. 2009, 48, 4572 –4576, DOI : 10.1002/anie.200901484 Link
6. Indoles from Simple Anilines and Alkynes : Palladium-Catalyzed C-H Activation Using Dioxygen as the Oxidant, Zhuangzhi Shi and Ning Jiao, Angew. Chem. Int. Ed. 2009, 48, 4572 –4576, DOI : 10.1002/anie.200901484
5. A Palladium-Catalyzed Oxidative Cycloaromatization of Biaryls with Alkynes Using Molecular Oxygen as the Oxidant, Zhuangzhi Shi and Ning Jiao, Angew. Chem. Int. Ed. 2009, 48, 7895 –7898, doi:10.1002/anie.200903975 Link
5. A Palladium-Catalyzed Oxidative Cycloaromatization of Biaryls with Alkynes Using Molecular Oxygen as the Oxidant, Zhuangzhi Shi and Ning Jiao, Angew. Chem. Int. Ed. 2009, 48, 7895 –7898, doi:10.1002/anie.200903975
2. Fe-catalyzed highly selective ring expansion of alkynylcyclopropyl alkanols to cyclobutanols, Anjun Chen and Ning Jiao, Chem. Commun., 2009, 6842–6844, doi:10.1039/b916623h Link
2. Fe-catalyzed highly selective ring expansion of alkynylcyclopropyl alkanols to cyclobutanols, Anjun Chen and Ning Jiao, Chem. Commun., 2009, 6842–6844, doi:10.1039/b916623h
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