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Collect. Czech. Chem. Commun. 2000, 65, 1777-1790
https://doi.org/10.1135/cccc20001777

Substituent Effects on the Base-Catalysed Hydrolysis of Phenyl Esters of para-Substituted Benzoic Acids

Ingrid Bauerová* and Miroslav Ludwig

Department of Organic Chemistry, Faculty of Chemical Technology, University of Pardubice, Čs. Legií 565, CZ-532 10 Pardubice, Czech Republic

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  • Nummert Vilve, Piirsalu Mare, Koppel Ilmar A.: Prediction of ortho substituent effect in alkaline hydrolysis of phenyl esters of substituted benzoic acids in aqueous acetonitrile. cent.eur.j.chem. 2013, 11, 1964. <https://doi.org/10.2478/s11532-013-0321-5>
  • Nummert Vilve, Mäemets Vahur, Piirsalu Mare, Koppel Ilmar A.: Influence of ortho substituents on 17O NMR chemical shifts in phenyl esters of substituted benzoic acids. J Phys Org Chem 2011, 24, 539. <https://doi.org/10.1002/poc.1784>
  • Nummert Vilve, Piirsalu Mare, Mäemets Vahur, Vahur Signe, Koppel Ilmar A.: Effect of ortho substituents on carbonyl carbon 13 C NMR chemical shifts in substituted phenyl benzoates. J. Phys. Org. Chem. 2009, 22, 1155. <https://doi.org/10.1002/poc.1569>
  • Nummert Vilve, Piirsalu Mare, Koppel Ilmar A.: Influence of solvent on the ortho substituent effect in the alkaline hydrolysis of phenyl esters of substituted benzoic acids. J. Phys. Org. Chem. 2009, 23, 497. <https://doi.org/10.1002/poc.1628>
  • Nummert Vilve, Piirsalu Mare, Vahur Signe, Travnikova Oksana, Koppel Ilmar A.: Kinetic study of hydrolysis of benzoates. part xxvii. ortho substituent effect in alkaline hydrolysis of phenyl esters of substituted benzoic acids in aqueous Bu4NBr. Collect. Czech. Chem. Commun. 2009, 74, 29. <https://doi.org/10.1135/cccc2008019>
  • Nummert Vilve, Piirsalu Mare, Mäemets Vahur, Koppel Ilmar: Kinetic Study of Hydrolysis of Benzoates. Part XXV. Ortho Substituent Effect in Alkaline Hydrolysis of Phenyl Esters of Substituted Benzoic Acids in Water. Collect. Czech. Chem. Commun. 2006, 71, 107. <https://doi.org/10.1135/cccc20060107>
  • Nummert Vilve, Piirsalu Mare, Mäemets Vahur, Koppel Ilmar: Kinetic study of hydrolysis of benzoates. Part XXIV—Variation of theortho substituent effect with solvent in the alkaline hydrolysis of substituted phenyl benzoates. J. Phys. Org. Chem. 2005, 18, 1138. <https://doi.org/10.1002/poc.967>
  • Oohashi Yoshiaki, Fukumoto Kentarou, Mukaiyama Teruaki: A New Method for the Synthesis of Carboxylic Esters and Lactones with Di-2-thienyl Carbonate (2-DTC) by the Promotion of DMAP and Iodine. BCSJ 2005, 78, 1508. <https://doi.org/10.1246/bcsj.78.1508>
  • Shintou Taichi, Fukumoto Kentaro, Mukaiyama Teruaki: Efficient Method for the Preparation of Inverted Alkyl Carboxylates and Phenyl Carboxylates via Oxidation–Reduction Condensation Using 2,6-Dimethyl-1,4-benzoquinone or Simple 1,4-Benzoquinone. BCSJ 2004, 77, 1569. <https://doi.org/10.1246/bcsj.77.1569>
  • Gundersen Lise-Lotte, Malterud Karl E, Negussie Ayele H, Rise Frode, Teklu Solomon, Østby Ole Benny: Indolizines as novel potent inhibitors of 15-Lipoxygenase. biorg med chem 2003, 11, 5409. <https://doi.org/10.1016/j.bmc.2003.09.033>
  • Gup Ramazan, Beduk A. Dincer: SYNTHESIS AND CHARACTERIZATION OF COMPLEXES OF Ni(II), Co(II), AND Cu(II) WITH FOUR 4-AMINOBENZOATE DERIVATIVES OF UNSYMMETRICAL vic-DIOXIMES. Synth React Inorg Met-org Chem 2002, 32, 1043. <https://doi.org/10.1081/SIM-120005621>
  • Nummert Vilve, Piirsalu Mare: Separation of ortho Inductive, Resonance and Steric Terms in Alkaline Hydrolysis of Substituted Phenyl Benzoates and Phenyl Tosylates. Collect. Czech. Chem. Commun. 2002, 67, 1833. <https://doi.org/10.1135/cccc20021833>
  • Bauerová Ingrid, Ludwig Miroslav: Substituent Effects on the Base-Catalysed Hydrolysis of Phenyl Esters of ortho-Substituted Benzoic Acids. Collect. Czech. Chem. Commun. 2001, 66, 770. <https://doi.org/10.1135/cccc20010770>