Bulletin of the Korean Chemical Society

  • 제32권11호
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  • Pages.4095-4098
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  • 2011
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Kinetics and Mechanism of the Aminolysis of Aryl N-Isopropyl Thiocarbamates in Acetonitrile

  • Oh, Hyuck-Keun (Department of Chemistry, Research Institute of Physics and Chemistry, Chonbuk National University)
  • 투고 : 2011.08.22
  • 심사 : 2011.09.16
  • 발행 : 2011.11.20
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참고문헌

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  1. Kinetics and Reaction Mechanism of Aminolyses of Benzyl 2-Pyridyl Carbonate and t-Butyl 2-Pyridyl Carbonate in Acetonitrile vol.33, pp.5, 2012, https://doi.org/10.5012/bkcs.2012.33.5.1547
  2. Kinetics and Reaction Mechanism of Aminolyses of Benzyl 2-Pyridyl Carbonate and t-Butyl 2-Pyridyl Carbonate: Effect of Nonleaving Group on Reactivity and Reaction Mechanism vol.33, pp.5, 2012, https://doi.org/10.5012/bkcs.2012.33.5.1551
  3. Aminolysis of Benzyl 2-Pyridyl Thionocarbonate and t-Butyl 2-Pyridyl Thionocarbonate: Effects of Nonleaving Groups on Reactivity and Reaction Mechanism vol.34, pp.4, 2013, https://doi.org/10.5012/bkcs.2013.34.4.1115
  4. A Kinetic Study on Ethylaminolysis of Phenyl Y-Substituted-Phenyl Carbonates: Effect of Leaving-Group Substituents on Reactivity and Reaction Mechanism vol.34, pp.6, 2013, https://doi.org/10.5012/bkcs.2013.34.6.1722
  5. Kinetics and Reaction Mechanism for Aminolysis of Benzyl 4-Pyridyl Carbonate in H2O: Effect of Modification of Nucleofuge from 2-Pyridyloxide to 4-Pyridyloxide on Reactivity and Reaction Me vol.33, pp.7, 2011, https://doi.org/10.5012/bkcs.2012.33.7.2269
  6. Aminolysis of Benzyl 4-Pyridyl Carbonate in Acetonitrile: Effect of Modification of Leaving Group from 2-Pyridyloxide to 4-Pyridyloxide on Reactivity and Reaction Mechanism vol.33, pp.8, 2011, https://doi.org/10.5012/bkcs.2012.33.8.2719