Kinetic investigation of the phenolysis of phenyl 4-nitrophenyl and phenyl 2,4-dinitrophenyl carbonates
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[1] E. Castro,et al. Concerted mechanisms of the reactions of methyl aryl carbonates with substituted phenoxide ions. , 2001, The Journal of organic chemistry.
[2] E. Castro. Kinetics and Mechanisms of Reactions of Thiol, Thiono, and Dithio Analogues of Carboxylic Esters with Nucleophiles. , 1999, Chemical reviews.
[3] E. Castro,et al. Kinetics and Mechanism of the Reactions of Quinuclidines with Ethyl S-Aryl Thiolcarbonates. , 1999, The Journal of organic chemistry.
[4] I. Um,et al. Effect of Solvent on the α-Effect: Nucleophilic Substitution Reactions of p-Nitrophenyl Acetate with m-Chlorophenoxide and Benzohydroxamates in MeCN−H2O Mixtures of Varying Compositions , 1997 .
[5] Andrew Williams,et al. The diagnosis of concerted organic mechanisms , 1994 .
[6] E. Castro,et al. Concerted mechanism of the reactions of secondary alicyclic amines with O-ethyl S-(2,4,6-trinitrophenyl) thiocarbonate , 1994 .
[7] W. Jencks,et al. Structure-reactivity correlations for reactions of substituted phenolate anions with acetate and formate esters , 1993 .
[8] A. Hengge. Can acyl transfer occur via a concerted mechanism ? Direct evidence from heavy-atom isotope effects , 1992 .
[9] E. Castro,et al. Concerted mechanism of the aminolysis of O-ethyl S-(2,4-dinitrophenyl) thiocarbonate , 1991 .
[10] Corwin Hansch,et al. A survey of Hammett substituent constants and resonance and field parameters , 1991 .
[11] I. Um,et al. Reaction Mechanism for Acyl-Transfer Reactions of Aryl Acetates with Aryloxides , 1990 .
[12] A. Luthra,et al. Concerted acetyl group transfer between substituted phenolate ion nucleophiles: variation of transition-state structure as a function of substituent , 1989 .
[13] E. Buncel,et al. Solvent-independent transition-state structure for acyl-transfer reactions. A novel strategy for construction of a Broensted correlation , 1989 .
[14] A. Luthra,et al. Concertedness in acyl group transfer in solution: a single transition state in acetyl group transfer between phenolate ion nucleophiles , 1987 .
[15] Andrew C. Williams,et al. A single transition state in the transfer of the methoxycarbonyl group between isoquinoline and substituted pyridines in aqueous solution , 1987 .
[16] W. Jencks,et al. Ester aminolysis. Partitioning of the tetrahedral addition intermediate, T.+-., and the relative leaving ability of nitrogen and oxygen , 1977 .
[17] W. Jencks,et al. Ester aminolysis. Structure-reactivity relationships and the rate-determining step in the aminolysis of substituted diphenyl carbonates , 1977 .
[18] W. Jencks,et al. Nonlinear structure-reactivity correlations. Acyl transfer between sulfur and oxygen nucleophiles , 1977 .
[19] W. Jencks,et al. The mechanism of the aminolysis of acetate esters. , 1974, Journal of the American Chemical Society.