Paper Publications

[61]guzhenhua.Pd/norbornene-catalyzed sequential ortho-C-H alkylation and ipso-alkynylation: a 1,1-dimethyl-2-alkynol strategy.ORGANIC CHEMISTRY FRONTIERS,2015,3(3):309-313.
[62]guzhenhua.Palladium-Catalyzed Catellani ortho-Acylation Reaction: An Efficient and Regiospecific Synthesis of Diaryl Ketones.ANGEWANDTE CHEMIE-INTERNATIONAL EDITION,2015,54(43):12669-12672.
[63]guzhenhua.BF3 center dot OEt2-Promoted Synthesis of 2,3-Metallocenocyclohexanones: A 1,2-Hydride Shift and Cationic Cyclization Strategy.JOURNAL OF ORGANIC CHEMISTRY,2015,80(16):7865-7875.
[64]guzhenhua.Palladium-Catalyzed Heck-type Domino Cyclization and Carboxylation to Synthesize Carboxylic Acids by Utilizing Chloroform as the Carbon Monoxide Source.JOURNAL OF ORGANIC CHEMISTRY,2015,80(15):7547-7554.
[65]guzhenhua.Decarboxylative Alkynyl Termination of Palladium-Catalyzed Catellani Reaction: A Facile Synthesis of alpha-Alkynyl Anilines via Ortho C-H Amination and Alkynylation.ORGANIC LETTERS,2015,17(9):2222-2225.
[66]guzhenhua.Stereoselective Synthesis of 1,3-Amino Alcohols by the Pd-Catalyzed Cyclization of Trichloroacetimidates.JOURNAL OF ORGANIC CHEMISTRY,2014,79(3):1289-1302.
[67]guzhenhua.N-Bromoacetamide-mediated domino cyclization and elimination of homoallylic trichloroacetimidates: a novel approach toward the synthesis of 1-bromo-2-amino-3-butene derivatives.ORGANIC & BIOMOLECULAR CHEMISTRY,2013,12(34):6653-6660.
[68]guzhenhua.Palladium-catalyzed intramolecular Cp-H bond functionalization/arylation: an enantioselective approach to planar chiral quinilinoferrocenes.RSC ADVANCES,2013,4(68):36241-36244.
[69]guzhenhua.Pd-Catalyzed Heck-Type Cascade Reactions with N-Tosyl Hydrazones: An Efficient Way to Alkenes via in Situ Generated Alkylpalladium.ORGANIC LETTERS,2013,15(18):4814-4817.
[70]Zhenhua Gu, Gregory B. Boursalian, Vincent Gandon, Robin Padilla, Hao Shen, Tatiana V. Timofeeva hayvan pornosuand K. Peter C. Vollhardt,* Yakovenko, A. A. Phenacenes from Phenylenes by Nickel-Catalyzed Alkyne Cycloadditions, Angew. Chem. Int. Ed. 2011, 50, 9413?9417.2011,

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