The Jiao Group

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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
34. An Efficient Approach to Alkenyl Nitriles from Allyl Esters Approach to Alkenyl Nitriles, Wang Zhou and Ning Jiao*, SYNLETT 2011, No. 7, pp 0887, DOI: 10.1055/s-0030-1259719 Link
34. An Efficient Approach to Alkenyl Nitriles from Allyl Esters Approach to Alkenyl Nitriles, Wang Zhou and Ning Jiao*, SYNLETT 2011, No. 7, pp 0887, DOI: 10.1055/s-0030-1259719
33. Copper-Catalyzed Aerobic Oxidative Coupling of Aryl Acetaldehydes with Anilines Leading to a-Ketoamides, Chun Zhang and Ning Jiao*, Angew. Chem. Int. Ed. 2011, 50, 11088, DOI : 10.1002/anie.201105285 Link
33. Copper-Catalyzed Aerobic Oxidative Coupling of Aryl Acetaldehydes with Anilines Leading to a-Ketoamides, Chun Zhang and Ning Jiao*, Angew. Chem. Int. Ed. 2011, 50, 11088, DOI : 10.1002/anie.201105285
32. Organocatalytic Asymmetric Intermolecular Dehydrogenative α-Alkylation of Aldehydes Using Molecular Oxygen as Oxidant, Bo Zhang and Ning Jiao*, Org. Lett., 2011, 13 (19), pp 5212–5215, DOI: 10.1021/ol202090a Link
32. Organocatalytic Asymmetric Intermolecular Dehydrogenative α-Alkylation of Aldehydes Using Molecular Oxygen as Oxidant, Bo Zhang and Ning Jiao*, Org. Lett., 2011, 13 (19), pp 5212–5215, DOI: 10.1021/ol202090a
31. Morpholine catalyzed direct C3 alkenylation of indoles with a,b-unsaturated aldehydes, Shi-Kai Xiang and Ning Jiao*, Chem. Commun., 2011, 47, 8097, DOI: 10.1039/c1cc12220g Link
31. Morpholine catalyzed direct C3 alkenylation of indoles with a,b-unsaturated aldehydes, Shi-Kai Xiang and Ning Jiao*, Chem. Commun., 2011, 47, 8097, DOI: 10.1039/c1cc12220g
30. The versatile roles of ammonium salt catalysts in enantioselective reduction and alkylation of a,b-unsaturated aldehydes: iminium catalysis,enamine catalysis and acid catalysis, Shi-Kai Xiang and Ning Jiao, Chem. Commun., 2011, 47, 5007 Link
30. The versatile roles of ammonium salt catalysts in enantioselective reduction and alkylation of a,b-unsaturated aldehydes: iminium catalysis,enamine catalysis and acid catalysis, Shi-Kai Xiang and Ning Jiao, Chem. Commun., 2011, 47, 5007
29. Iron-facilitated direct oxidative C–H transformation of allyl arenes to alkenyl aldehydes, Teng Wang, Li-He Zhang and Ning Jiao*, Tetrahedron Letters 52 (2011) 3208–3211, doi:10.1016/j.tetlet.2011.04.041 Link
29. Iron-facilitated direct oxidative C–H transformation of allyl arenes to alkenyl aldehydes, Teng Wang, Li-He Zhang and Ning Jiao*, Tetrahedron Letters 52 (2011) 3208–3211, doi:10.1016/j.tetlet.2011.04.041
28. Utilization of Natural Sunlight and Air in the Aerobic Oxidation of Benzyl Halides, Yijin Su, Liangren Zhang and Ning Jiao*, Org. Lett., 2011, 13 (9), pp 2168–2171, DOI: 10.1021/ol2002013 Link
28. Utilization of Natural Sunlight and Air in the Aerobic Oxidation of Benzyl Halides, Yijin Su, Liangren Zhang and Ning Jiao*, Org. Lett., 2011, 13 (9), pp 2168–2171, DOI: 10.1021/ol2002013
27. Inexpensive Copper/Iron-Cocatalyzed Reactions, Yijin Su and Ning Jiao*, SYNTHESIS 2011, No. 11, pp 1678–1690x, DOI: 10.1055/s-0030-1260028 Link
27. Inexpensive Copper/Iron-Cocatalyzed Reactions, Yijin Su and Ning Jiao*, SYNTHESIS 2011, No. 11, pp 1678–1690x, DOI: 10.1055/s-0030-1260028
26. Iron-Catalyzed C[BOND]H and C[BOND]C Bond Cleavage: A Direct Approach to Amides from Simple Hydrocarbons, Chong Qin and Ning Jiao*, Angew. Chem. Int. Ed. 2011, 50, 12595, DOI : 10.1002/anie.201106112 Link
26. Iron-Catalyzed C[BOND]H and C[BOND]C Bond Cleavage: A Direct Approach to Amides from Simple Hydrocarbons, Chong Qin and Ning Jiao*, Angew. Chem. Int. Ed. 2011, 50, 12595, DOI : 10.1002/anie.201106112
25. Phosphane-Free Copper-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids with Aryl Halides under Aerobic Conditions, Delin Pan and Ning Jiao*, Eur. J. Org. Chem. 2011, 4751–4755, DOI: 10.1002/ejoc.201100659 Link
25. Phosphane-Free Copper-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids with Aryl Halides under Aerobic Conditions, Delin Pan and Ning Jiao*, Eur. J. Org. Chem. 2011, 4751–4755, DOI: 10.1002/ejoc.201100659
24. An Efficient Difluorohydroxylation of Indoles Using Selectfluor as a Fluorinating Reagent, Riyuan Lin and Ning Jiao*, Org. Lett., 2011, 13 (17), pp 4498, DOI: 10.1021/ol201896p Link
24. An Efficient Difluorohydroxylation of Indoles Using Selectfluor as a Fluorinating Reagent, Riyuan Lin and Ning Jiao*, Org. Lett., 2011, 13 (17), pp 4498, DOI: 10.1021/ol201896p
23. Direct Transformation of N,N-Dimethylformamide to −CN: Pd-Catalyzed Cyanation of Heteroarenes via C–H Functionalization, Shengtao Ding and Ning Jiao*, J. Am. Chem. Soc., 2011, 133 (32), pp 12374–12377, DOI: 10.1021/ja204063z Link
23. Direct Transformation of N,N-Dimethylformamide to −CN: Pd-Catalyzed Cyanation of Heteroarenes via C–H Functionalization, Shengtao Ding and Ning Jiao*, J. Am. Chem. Soc., 2011, 133 (32), pp 12374–12377, DOI: 10.1021/ja204063z
22. Implanting Nitrogen into Hydrocarbon Molecules through C-H and C-C Bond Cleavages : A Direct Approach to Tetrazoles, Feng Chen and Ning Jiao, Angew. Chem. Int. Ed. 2011, 50, 11487, DOI : 10.1002/anie.201105505 Link
22. Implanting Nitrogen into Hydrocarbon Molecules through C-H and C-C Bond Cleavages : A Direct Approach to Tetrazoles, Feng Chen and Ning Jiao, Angew. Chem. Int. Ed. 2011, 50, 11487, DOI : 10.1002/anie.201105505
21. An Efficient Transformation from Benzyl or Allyl Halides to Aryl and Alkenyl Nitriles, Wang Zhou and Ning Jiao*, Org. Lett., 2010, 12 (12), pp 2888–2891, DOI: 10.1021/ol101094u Link
21. An Efficient Transformation from Benzyl or Allyl Halides to Aryl and Alkenyl Nitriles, Wang Zhou and Ning Jiao*, Org. Lett., 2010, 12 (12), pp 2888–2891, DOI: 10.1021/ol101094u
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
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