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Effect of solvent on reactivity and basicity: aminolyses of p-nitrophenyl acetate in H<sub>2</sub>O and in DMSO.
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- Journal of Physical Organic Chemistry, 2002, v. 15, n. 8, p. 561, doi. 10.1002/poc.483
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- Article
Effect of solvent composition on the acidity of phenols in dimethyl sulfoxide-water mixtures.
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- Journal of Physical Organic Chemistry, 1998, v. 11, n. 12, p. 847, doi. 10.1002/(SICI)1099-1395(199812)11:12<847::AID-POC42>3.0.CO;2-5
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- Article
Kinetic study on aminolysis of aryl X-substituted-cinnamates in acetonitrile: differential medium effect determines reactivity and reaction mechanism.
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- Canadian Journal of Chemistry, 2019, v. 97, n. 1, p. 13, doi. 10.1139/cjc-2018-0310
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- Article
Hydrazinolysis of aryl cinnamates and related esters: the α-effect arises from stabilization of five-membered cyclic transition state.
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- Canadian Journal of Chemistry, 2019, v. 97, n. 1, p. 7, doi. 10.1139/cjc-2018-0290
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- Article
Unexpected medium effect on the mechanism for aminolysis of aryl phenyl carbonates in acetonitrile and H2O: transition-state structure in the catalytic pathway.
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- Canadian Journal of Chemistry, 2018, v. 96, n. 12, p. 1011, doi. 10.1139/cjc-2018-0204
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- Article
Medium effect on the α-effect for nucleophilic substitution reactions of p-nitrophenyl acetate with benzohydroxamates and m-chlorophenoxide in DMSO–H2O mixtures as contrasts with MeCN–H2O mixtures: comparing two very different polar aprotic solvent components.
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- Canadian Journal of Chemistry, 2018, v. 96, n. 10, p. 922, doi. 10.1139/cjc-2018-0103
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- Article
Medium effect (water versus MeCN) on reactivity and reaction pathways for the S<sub>N</sub>Ar reaction of 1-aryloxy-2,4-dinitrobenzenes with cyclic secondary amines.
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- Canadian Journal of Chemistry, 2017, v. 95, n. 12, p. 1273, doi. 10.1139/cjc-2017-0454
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- Article
Alkali metal ion catalysis and inhibition in alkaline ethanolysis of O-Y-substituted-phenyl O-phenyl thionocarbonates: contrasting M<sup>+</sup> ion effects upon changing electrophilic centre from C=O to C=S.
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- Canadian Journal of Chemistry, 2017, v. 95, n. 1, p. 45, doi. 10.1139/cjc-2016-0378
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- Article
The α-effect in the S<sub>N</sub>Ar reaction of 1-(4-nitrophenoxy)-2,4-dinitrobenzene with anionic nucleophiles: effects of solvation and polarizability on the α-effect.
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- Canadian Journal of Chemistry, 2015, v. 93, n. 10, p. 1109, doi. 10.1139/cjc-2015-0073
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- Article
Kinetic Study on Alkaline Hydrolysis of 2-Pyridyl and 4-Pyridyl X-substituted-Benzoates: Effects of Benzoyl Substituent X and Leaving-Group Basicity on Reactivity and Reaction Mechanism.
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- Bulletin of the Korean Chemical Society, 2017, v. 38, n. 10, p. 1138, doi. 10.1002/bkcs.11233
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- Article
Kinetic Study on Nucleophilic Substitution Reactions of O-Phenyl O-Y-substituted-Phenyl Thionocarbonates with 1,8-Diazabicyclo[5.4.0]undec-7-ene in Acetonitrile.
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- Bulletin of the Korean Chemical Society, 2017, v. 38, n. 10, p. 1169, doi. 10.1002/bkcs.11242
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- Article
Kinetic Study on Quinuclidinolysis of O-Phenyl O-Y-substituted-Phenyl Thionocarbonates: Effects of Changing Nonleaving Group from Thionobenzoyl to Phenyloxythionocarbonyl on Reactivity and Transition-State Structure.
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- Bulletin of the Korean Chemical Society, 2017, v. 38, n. 9, p. 1091, doi. 10.1002/bkcs.11227
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- Article
Alkaline Hydrolysis of 4-Nitrophenyl X-Substituted-Benzoates Revisited: New Insights from Yukawa-Tsuno Equation.
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- Bulletin of the Korean Chemical Society, 2016, v. 37, n. 12, p. 2062, doi. 10.1002/bkcs.11000
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- Article
Kinetic Study on Aminolysis of 4-Pyridyl Benzoate and O-4-Pyridyl Thionobenzoate in Acetonitrile: Factors Influencing Reactivity and Reaction Mechanism.
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- Bulletin of the Korean Chemical Society, 2016, v. 37, n. 10, p. 1577, doi. 10.1002/bkcs.10906
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- Article
Kinetic Study on Aminolysis of O-2-Pyridyl Thionobenzoate in Acetonitrile: Effect of Changing Electrophilic Center from CO to CS on Reactivity and Reaction Mechanism.
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- Bulletin of the Korean Chemical Society, 2016, v. 37, n. 9, p. 1401, doi. 10.1002/bkcs.10875
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- Article
Kinetic Study on Nucleophilic Substitution Reactions of Aryl Diphenylphosphinates with Butane-2,3-dione Monoximate and Aryloxide Anions: Reaction Mechanism and Origin of the α-Effect.
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- Bulletin of the Korean Chemical Society, 2016, v. 37, n. 8, p. 1180, doi. 10.1002/bkcs.10836
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- Article
Kinetic Study on Nucleophilic Displacement Reactions of Phenyl Y-Substituted Phenyl Carbonates with 1,8-Diazabicyclo[5.4.0]undec-7-ene: Effects of Amine Nature on Reaction Mechanism.
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- Bulletin of the Korean Chemical Society, 2016, v. 37, n. 1, p. 77, doi. 10.1002/bkcs.10627
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- Article
S<sub>N</sub>Ar Reactions of 1-Halo-2,4-dinitrobenzenes with Alkali-Metal Ethoxides: Differential Stabilization of Ground State and Transition State Determines Alkali-Metal Ion Catalysis or Inhibition.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 7, p. 1812, doi. 10.1002/bkcs.10344
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- Article
Kinetic Study on S<sub>N</sub>Ar Reactions of 1-(Y-Substituted-phenoxy)-2,4-dinitrobenzenes with Azide Ion: Effect of Changing Nucleophile from Hydroxide to Azide Ion on Reaction Mechanism and Reactivity.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 7, p. 1764, doi. 10.1002/bkcs.10333
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- Article
Kinetic Study on Quinuclidinolysis of O-4-Nitrophenyl X-substituted Thionobenzoates and O-3,4-Dinitrophenyl Thionobenzoate: Effect of Amine Nature on Reactivity and Reaction Mechanism.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 6, p. 1551, doi. 10.1002/bkcs.10293
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- Article
Kinetic Study on Alkaline Hydrolysis of Y-substituted Phenyl X-substituted Benzenesulfonates: Effects of Changing Nucleophile from Azide to Hydroxide Ion on Reactivity and Transition-State Structure.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 6, p. 1563, doi. 10.1002/bkcs.10297
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- Article
Nucleophilic Substitution Reactions of 2,4-Dinitrophenyl X-Substituted-Benzenesulfonates and Y-Substituted-Phenyl 4-Nitrobenzenesulfonates with Azide Ion: Regioselectivity and Reaction Mechanism.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 5, p. 1360, doi. 10.1002/bkcs.10259
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- Article
Kinetic and Mechanistic Studies on Quinuclidinolysis of Y-substituted-Phenyl Picolinates: Effect of Amine Nature on Reactivity and Transition-State Structure.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 5, p. 1405, doi. 10.1002/bkcs.10272
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- Article
Kinetic Study on Alkaline Hydrolysis of Y-substituted Phenyl Picolinates: Effects of Modification of Nonleaving Group from Benzoyl to Picolinyl on Reactivity and Reaction Mechanism.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 4, p. 1138, doi. 10.1002/bkcs.10211
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- Article
Kinetic Study on Reactions of O- Y-substituted Phenyl Thionobenzoates with Quinuclidine: Factors Governing Reactivity and Reaction Mechanism.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 4, p. 1120, doi. 10.1002/bkcs.10207
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- Article
Kinetic study on pyridinolysis of aryl benzenesulfonates: factors governing regioselectivity and reaction mechanism.
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- Canadian Journal of Chemistry, 2022, v. 100, n. 5, p. 378, doi. 10.1139/cjc-2021-0287
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- Article
Effect of medium on reactivity for alkaline hydrolysis of p-nitrophenyl acetate and S-p-nitrophenyl thioacetate in DMSO–H<sub>2</sub>O mixtures of varying compositions: ground state and transition state contributions.
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- Canadian Journal of Chemistry, 2021, v. 99, n. 6, p. 557, doi. 10.1139/cjc-2020-0503
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- Article
Effects on the Reactivity by Changing the Electrophilic Center from CO to CS: Contrasting Reactivity of Hydroxide, p-Chlorophenoxide, and Butan-2,3-dione Monoximate in DMSO/H<sub>2</sub>O Mixtures.
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- Chemistry - A European Journal, 2009, v. 15, n. 4, p. 1011, doi. 10.1002/chem.200801534
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- Article
Analysis of Linear Free-Energy Relationships Combined with Activation Parameters Assigns a Concerted Mechanism to Alkaline Hydrolysis of X-Substituted Phenyl Diphenylphosphinates.
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- Chemistry - A European Journal, 2008, v. 14, n. 24, p. 7324, doi. 10.1002/chem.200800553
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- Article
Multiparameter kinetic analysis of alkaline hydrolysis of a series of aryl diphenylphosphinothioates: models for P=S neurotoxins.
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- Journal of Physical Organic Chemistry, 2017, v. 30, n. 7, p. n/a, doi. 10.1002/poc.3657
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- Article
Alkali-Metal Ion Catalysis and Inhibition in S<sub>N</sub>Ar Displacement: Relative Stabilization of Ground State and Transition State Determines Catalysis and Inhibition in S<sub>N</sub>Ar Reactivity.
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- Chemistry - A European Journal, 2014, v. 20, n. 41, p. 13337, doi. 10.1002/chem.201404004
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- Article
Alkali-Metal-Ion Catalysis and Inhibition in the Nucleophilic Displacement Reaction of Y-Substituted Phenyl Diphenylphosphinates and Diphenylphosphinothioates with Alkali-Metal Ethoxides: Effect of Changing the Electrophilic Center from PO to PS
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- Chemistry - A European Journal, 2012, v. 18, n. 3, p. 961, doi. 10.1002/chem.201102404
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- Article
Kinetic and Theoretical Studies on Alkaline Ethanolysis of 4-Nitrophenyl Salicylate: Effect of Alkali Metal Ions on Reactivity and Mechanism.
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- Chemistry - A European Journal, 2011, v. 17, n. 10, p. 3021, doi. 10.1002/chem.201002692
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- Article