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成佳佳
2023-05-10 10:32
  • 成佳佳
  • 成佳佳 - -福州大学-化学学院-个人资料

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Lu, B.*; Lu, Q.; Zhuang, S.; Cheng, J.*; Huang, B. Bi(OTf)3-catalyzed C-H Bond Functionalization of Azaarenes for the Facile Access to Oxindoles Featuring Quaternary Carbon Centers. RSC Advances, 2015, 5, 8285-8288.
Namitharan, K.¶; Zhu, T.¶; Cheng, J.; Zheng, P.; Li, X.; Yang, S.; Song, B.; Chi, Y. Robin.* (¶ contributed equally). Metal and Carbene OrganocatalyticRelay Activation of Alkynes for Stereoselective Reactions. Nature Communications 2014, 5, 3982.
Cheng, J.; Huang, Z.; Chi, Y. Robin.* NHC Organocatalytic Formal LUMO Activation of α,β-Unsaturated Esters for Reaction with Enamides. Angewandte Chemie International Edition 2013, 52, 8592-8596.
Cheng, J.; Tang,X.; Ma, S.* Highly Selective FeCl3-Catalyzed Cyclization of β-Sulfonamidoallenes or β-Allenols and Aldehydes. ACS Catalysis 2013, 3, 663-666.
Cheng, J.; Tang,X.; Ma, S.* FeCl3-Catalyzed Cyclization of α-Amino Allenes and Aldehydes: The Substituent Effect. Chemical Communications 2012, 48, 12074-12076.
Cheng, J.; Jiang, X.; Ma, S.* Palladium-Catalyzed Approach to Stereodefined Ten-Membered Cycles from 1,5-Bisallenes. Organic Letters 2011, 13, 5200-5203.
Cheng, J.; Jiang, X.; Zhu, C.; Ma, S.* Palladium-Catalyzed Three-Component Tandem Cyclization Reaction of 2-(2,3-Allenyl)acylacetates, Organic Halides, and Amines: An Effective Protocol for the Synthesis of 4,5-Dihydro-1H-pyrrole Derivatives. Advanced Synthesis & Catalysis 2011, 353, 1676-1682.
Ma, S.*; Liu, J.; Li, S.; Chen, B.; Cheng, J.; Kuang, J.; Liu, Y.; Wan, B.; Wang, Y.; Ye, J.; Y, Q.; Yuan, W.; Yu, S. Development of a General and Practical Iron Nitrate/TEMPO-Catalyzed Aerobic Oxidation of Alcohols to Aldehydes/Ketones: Catalysis with Table Salt. Advanced Synthesis & Catalysis 2011, 353, 1005-1017.
Peng, C.; Cheng, J.; Wang, J.* Sequential Copper(I)-Catalyzed Reaction of Amines with o-Acetyl-enyl-Substituted Phenyldiazoacetates. Advanced Synthesis & Catalysis 2008, 350, 2359-2364.
Peng, C.;Cheng, J.; Wang, J.* Palladium-Catalyzed Cross-Coupling of Aryl or Vinyl Iodides with Ethyl Diazoacetate. Journal of the American Chemical Society 2007, 129, 8708-8709.

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