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Chemistry Experts

Jinhong Lin

Professor
Department of Chemistry
Institute of Organic Chemistry
China

Biography

Education and Appointments: 03/2013-present: Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences. 03/2011–02/2013: State University of New York at Albany. Postdoctoral Fellow, advisor: John T. Welch. 09/2005–01/2011: Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences. Ph. D., advisor: Ji-Chang Xiao. 09/2001–07/2005: Donghua Univeristy, bachelor.

Research Interest

1.The development of novel organofluorinated salts and the application of them into fluoroalkylation 2.Asymmetric fluorination and fluoroalkylation.

Publications

  • Lin, J.-H.; Zhang, C.-P.; Xiao, J.-C.; “Enantioselective Aldol Reaction of Cyclic Ketones with Aryl Aldehydes Catalyzed by Cyclohexanediamine Derived Salt in the Presence of Water”; Green Chem., 2009, 11, 1750.

  • Lin, J.-H.; Xiao, J.-C.; “The Asymmetric Friedel–Crafts Reaction of Indoles with Fluoroalkylated Nitroalkenes Catalyzed by Chiral Phosphoric Acid”; Eur. J. Org. Chem., 2011, 4536.

  • Savoie, P. R.; Higashiya, S.; Lin, J.-H.; Wagle, D. V.; Welch, J. T.; “Conformational impact of pentafluorosulfanylation on acyclic aliphatic molecules”; J. Fluorine Chem., 2012,143, 281.

  • Ngo,S. C.; Lin, J.-H.; Savoie, P. R.; Hines, E. M.; Pugliese, K. M.; Welch, J. T.; “ Preparation and Reactions of Aliphatic 2-Pentafluorosulfanyl Aldehydes”; Eur. J. Org. Chem., 2012, 4902.

  • Ngo,S. C.; Lin, J.-H.; Savoie, P. R.; Hines, E. M.; Pugliese, K. M.; Welch, J. T.; “ Preparation and Reactions of Aliphatic 2-Pentafluorosulfanyl Aldehydes”; Eur. J. Org. Chem., 2012, 4902.

  • Lim, D.-S.; Lin, J.-H.; Welch, J. T.; “The Synthesis and Characterization of a Pentafluorosulfanylated Peptide”; Eur. J. Org. Chem., 2012, 3946.

  • Lin, J.-H.; Zong, G.; Du, R.-B.; Xiao, J.-C.; Liu, S.; “The asymmetric synthesis of CF3- or -CF2- substituted tetrahydroquinolines by employing chiral phosphoric acid as catalyst”; Chem. Comm., 2012,48, 7738.

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