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Results: 1-8 |
Results: 8
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
Deprotonation of the alpha-(N,N-dimethylcarbamoyl)-alpha-methyl-4methoxybenzyl carbocation by alkanecarboxylate and halide ions
Authors: Toteva, MM Richard, JP
Citation: Mm. Toteva et Jp. Richard, Deprotonation of the alpha-(N,N-dimethylcarbamoyl)-alpha-methyl-4methoxybenzyl carbocation by alkanecarboxylate and halide ions, J CHEM S P2, (7), 2001, pp. 1167-1173
Changes in the relative contribution of specific and general base catalysis in cationic micelles. The cyclization of substituted ethyl hydantoates
Authors: Blagoeva, IB Toteva, MM Ouarti, N Ruasse, MF
Citation: Ib. Blagoeva et al., Changes in the relative contribution of specific and general base catalysis in cationic micelles. The cyclization of substituted ethyl hydantoates, J ORG CHEM, 66(6), 2001, pp. 2123-2130
A normal gem-dimethyl effect in the base-catalyzed cyclization of omega-(p-nitrophenyl)hydantoic acids: evidence for hindered proton transfer in the permethylated esters
Authors: Blagoeva, IB Kirby, AJ Kochiyashki, II Koedjikov, AH Pojarlieff, IG Toteva, MM
Citation: Ib. Blagoeva et al., A normal gem-dimethyl effect in the base-catalyzed cyclization of omega-(p-nitrophenyl)hydantoic acids: evidence for hindered proton transfer in the permethylated esters, J CHEM S P2, (9), 2000, pp. 1953-1960
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
Assisted hydrolysis of cis-2-(3-phenylthioureido) cyclopentane-carbonitrile in alkaline solution. Solvent dependent switch from hydrolysis to rearrangement of the iminothiooxopyrimidine intermediate
Authors: Atay, E Blagoeva, IB Chubb, FL Edward, JT Pojarlieff, IG Toteva, MM
Citation: E. Atay et al., Assisted hydrolysis of cis-2-(3-phenylthioureido) cyclopentane-carbonitrile in alkaline solution. Solvent dependent switch from hydrolysis to rearrangement of the iminothiooxopyrimidine intermediate, CAN J CHEM, 78(1), 2000, pp. 84-94
Structure-reactivity relationships and intrinsic reaction barriers for nucleophile additions to a quinone methide: A strongly resonance-stabilized carbocation
Authors: Richard, JP Toteva, MM Crugeiras, J
Citation: Jp. Richard et al., Structure-reactivity relationships and intrinsic reaction barriers for nucleophile additions to a quinone methide: A strongly resonance-stabilized carbocation, J AM CHEM S, 122(8), 2000, pp. 1664-1674
Structure-reactivity relationships for addition of sulfur nucleophiles to electrophilic carbon: Resonance, polarization, and steric/electrostatic effects
Authors: Toteva, MM Richard, JP
Citation: Mm. Toteva et Jp. Richard, Structure-reactivity relationships for addition of sulfur nucleophiles to electrophilic carbon: Resonance, polarization, and steric/electrostatic effects, J AM CHEM S, 122(45), 2000, pp. 11073-11083
Risultati: 1-8 |