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Results: 1-10 |
Results: 10
Dynamics for reaction of an ion pair in aqueous solution: Reactivity of carboxylate anions in bimolecular carbocation-nucleophile addition and unimolecular ion pair collapse
Authors: Tsuji, Y Mori, T Richard, JP Amyes, TL Fujio, M Tsuno, Y
Citation: Y. Tsuji et al., Dynamics for reaction of an ion pair in aqueous solution: Reactivity of carboxylate anions in bimolecular carbocation-nucleophile addition and unimolecular ion pair collapse, ORG LETT, 3(8), 2001, pp. 1237-1240
What is the stabilizing interaction with nucleophilic solvents in the transition state for solvolysis of tertiary derivatives: Nucleophilic solvent participation or nucleophilic solvation?
Authors: Richard, JP Toteva, MM Amyes, TL
Citation: Jp. Richard et al., 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, 3(14), 2001, pp. 2225-2228
Proton transfer at carbon
Authors: Richard, JP Amyes, TL
Citation: Jp. Richard et Tl. Amyes, Proton transfer at carbon, CURR OP C B, 5(6), 2001, pp. 626-633
Contribution of phosphate intrinsic binding energy to the enzymatic rate acceleration for triosephosphate isomerase
Authors: Amyes, TL O'Donoghue, AC Richard, JP
Citation: Tl. Amyes et al., Contribution of phosphate intrinsic binding energy to the enzymatic rate acceleration for triosephosphate isomerase, J AM CHEM S, 123(45), 2001, pp. 11325-11326
Glycine enolates: The large effect of iminium ion formation on alpha-aminocarbon acidity
Authors: Rios, A Crugeiras, J Amyes, TL Richard, JP
Citation: A. Rios et al., Glycine enolates: The large effect of iminium ion formation on alpha-aminocarbon acidity, J AM CHEM S, 123(32), 2001, pp. 7949-7950
How does structure determine organic reactivity? Partitioning of carbocations between addition of nucleophiles and deprotonation
Authors: Richard, JP Amyes, TL Lin, SS O'Donoghue, AC Toteva, MM Tsuji, Y Williams, KB
Citation: Jp. Richard et al., How does structure determine organic reactivity? Partitioning of carbocations between addition of nucleophiles and deprotonation, ADV PHYS O, 35, 2000, pp. 67-115
Formation and stability of organic zwitterions in aqueous solution: Enolates of the amino acid glycine and its derivatives
Authors: Rios, A Amyes, TL Richard, JP
Citation: A. Rios et al., Formation and stability of organic zwitterions in aqueous solution: Enolates of the amino acid glycine and its derivatives, J AM CHEM S, 122(39), 2000, pp. 9373-9385
How does organic structure determine organic reactivity? The effect of ortho-dimethyl groups on the nucleophilic substitution and alkene-forming elimination reactions of ring-substituted cumyl derivatives
Authors: Amyes, TL Mizerski, T Richard, JP
Citation: Tl. Amyes et al., How does organic structure determine organic reactivity? The effect of ortho-dimethyl groups on the nucleophilic substitution and alkene-forming elimination reactions of ring-substituted cumyl derivatives, CAN J CHEM, 77(5-6), 1999, pp. 922-933
Intrinsic barriers for the reactions of an oxocarbenium ion in water
Authors: Richard, JP Williams, KB Amyes, TL
Citation: Jp. Richard et al., Intrinsic barriers for the reactions of an oxocarbenium ion in water, J AM CHEM S, 121(36), 1999, pp. 8403-8404
Intrinsic barriers to the formation and reaction of carbocations
Authors: Richard, JP Amyes, TL Williams, KB
Citation: Jp. Richard et al., Intrinsic barriers to the formation and reaction of carbocations, PUR A CHEM, 70(10), 1998, pp. 2007-2014
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