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Pure Appl. Chem., 1998, Vol. 70, No. 10, pp. 2023-2030

http://dx.doi.org/10.1351/pac199870102023

Structural modification and solvent interactions in solvolytic reactions of open-chain compounds

K. Takeuchi

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  • Takeuchi Ken'ichi: ChemInform Abstract: Structural Modification and Solvent Interactions in Solvolytic Reactions of Open-Chain Compounds. ChemInform 2010, 30, no. <http://dx.doi.org/10.1002/chin.199928327>
  • Ponomarev N. E., Zaliznyi V. V., Dvorko G. F.: Kinetics and mechanism of monomolecular heterolysis of commercial organohalogen compounds: XLIII. Solvent effect on activation parameters of dehydrochlorination of 3-chloro-3-methylbut-1-ene. Correlation analysis of solvation effects. Russ J Gen Chem 2007, 77, 1204. <http://dx.doi.org/10.1134/S1070363207070110>
  • Takeuchi Ken'ichi, Takasuka Masaaki, Shiba Eiji, Tokunaga Hironobu, Endo Tadasuke, Ushino Takuhiro, Tokunaga Kazuhiko, Okazaki Takao, Kinoshita Tomomi, Ohga Yasushi: The Grunwald-Winstein relationship in the solvolysis of crowded tertiary alkyl chlorides. Hindered hydration and hydrophobic effect. J Phys Org Chem 2001, 14, 229. <http://dx.doi.org/10.1002/poc.358>
  • Richard John P., Toteva Maria M., Amyes Tina L.: What Is the Stabilizing Interaction with Nucleophilic Solvents in the Transition State for Solvolysis of Tertiary Derivatives:  Nucleophilic Solvent Participation or Nucleophilic Solvation?. Org Lett 2001, 3, 2225. <http://dx.doi.org/10.1021/ol016103j>
  • Müller Paul, Rossier Jean-Claude, Abboud Jose-Luis M.: Gas-phase stability of tertiary carbenium ions and rates of solvolysis of tertiary derivatives. J Phys Org Chem 2000, 13, 569. <http://dx.doi.org/10.1002/1099-1395(200010)13:10<569::AID-POC274>3.0.CO;2-H>
  • Liu Kwang-Ting, Chang Chih-Wei, Chen Hung-I, Chin Chien-Pu, Duann Yeh-Fang: Solvolysis of 2-aryl-2-adamantylp-nitrobenzoates and some tertiary benzylicp-nitrobenzoates.YBnOPNB andYxBnOPNB scales. J Phys Org Chem 2000, 13, 203. <http://dx.doi.org/10.1002/(SICI)1099-1395(200004)13:4<203::AID-POC230>3.0.CO;2-9>