The Jiao Group

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10. Direct Transformation of Methyl Arenes to Aryl Nitriles at Room Temperature, Wang Zhou, Liangren Zhang, and Ning Jiao, Angew. Chem. Int. Ed. 2009, 48, 7094 –7097, DOI : 10.1002/anie.200903838 Link
10. Direct Transformation of Methyl Arenes to Aryl Nitriles at Room Temperature, Wang Zhou, Liangren Zhang, and Ning Jiao, Angew. Chem. Int. Ed. 2009, 48, 7094 –7097, DOI : 10.1002/anie.200903838
9. The tandem reaction combining radical and ionic processes: an efficient approach to substituted 3,4-dihydroquinolin-2-ones, Wang Zhou and Ning Jiao, Tetrahedron 65 (2009) 1982–1987, doi:10.1016/j.tet.2009.01.027 Link
9. The tandem reaction combining radical and ionic processes: an efficient approach to substituted 3,4-dihydroquinolin-2-ones, Wang Zhou and Ning Jiao, Tetrahedron 65 (2009) 1982–1987, doi:10.1016/j.tet.2009.01.027
8. Sp–sp3 C–C bond formation viaFe(OTf)3/TfOH cocatalyzed coupling reaction of terminal alkynes with benzylic alcohols, Shi-Kai Xiang,Li-He Zhang and Ning Jiao*, Chem. Commun., 2009, 6487–6489.doi: 10.1039/b911905a Link
8. Sp–sp3 C–C bond formation viaFe(OTf)3/TfOH cocatalyzed coupling reaction of terminal alkynes with benzylic alcohols, Shi-Kai Xiang,Li-He Zhang and Ning Jiao*, Chem. Commun., 2009, 6487–6489.doi: 10.1039/b911905a
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
4. Copper/Iron-Cocatalyzed Highly Selective Tandem Reactions : Efficient Approaches to Z-g-Alkylidene Lactones, Si Li, Wei Jia and Ning Jiao, Adv. Synth. Catal. 2009, 351, 569 – 575, doi: 10.1002/adsc.200800695 Link
4. Copper/Iron-Cocatalyzed Highly Selective Tandem Reactions : Efficient Approaches to Z-g-Alkylidene Lactones, Si Li, Wei Jia and Ning Jiao, Adv. Synth. Catal. 2009, 351, 569 – 575, doi: 10.1002/adsc.200800695
3. AgNO3 catalyzed cyclization of propargyl-Meldrum’s acids in aqueous solvent: highly selective synthesis of Z-γ-alkylidene lactones, Wei Jia and Ning Jiao, Tetrahedron Letters 50 (2009) 5406–5408, doi:10.1016/j.tetlet.2009.07.050 Link
3. AgNO3 catalyzed cyclization of propargyl-Meldrum’s acids in aqueous solvent: highly selective synthesis of Z-γ-alkylidene lactones, Wei Jia and Ning Jiao, Tetrahedron Letters 50 (2009) 5406–5408, doi:10.1016/j.tetlet.2009.07.050
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