Year |
Citation |
Score |
1965 |
Godfrey TS, Hughes ED, Ingold C. 190. Homolytic substitution at a saturated carbon atom. Part III. Kinetics of the gaseous reaction of nitric acid in nitrogen alone and in the presence of methane Journal of the Chemical Society (Resumed). 1063-1079. DOI: 10.1039/Jr9650001063 |
0.766 |
|
1964 |
Banthorpe DV, Hughes ED, Ingold C, Bramley R, Thomas JA. 560. Mechanism of benzidine and semidine rearrangements. Part XV. A collective discussion Journal of the Chemical Society (Resumed). 2864-2901. DOI: 10.1039/Jr9640002864 |
0.668 |
|
1964 |
Banthorpe DV, Hughes ED, Ingold C, Bramley R, Thomas JA. Mechanism of benzidine and semidine rearrangements. Part XV. A collective discussion Journal of the Chemical Society (Resumed). 2860-2864. |
0.641 |
|
1964 |
Hoffmann HMR, Hughes ED. Reaction kinetics and the waiden inversion. Part XI. Steric course of bimolecular nucleophilic substitution by a neutral nucleophile on a neutral substrate Journal of the Chemical Society (Resumed). 1249-1251. |
0.345 |
|
1964 |
Hughes ED, Ingold CK, Roberts RMG. Mechanism of electrophilic substitution at a saturated carbon atom. Part VII. Kinetics and stereochemistry of a one-alkyl mercury exchange, which has bimolecular and unimolecular mechanisms, as well as anion-catalysed derivative mechanisms Journal of the Chemical Society (Resumed). 3897-3899. |
0.748 |
|
1962 |
Banthorpe DV, Hughes ED, Ingold C, Humberlin R. 653. Mechanism of benzidine and semidine rearrangements. Part IX. Substrate-isotope effects on kinetics and products of acid rearrangement of 1,1′-hydrazonaphthalene Journal of the Chemical Society (Resumed). 3299-3308. DOI: 10.1039/Jr9620003299 |
0.664 |
|
1962 |
Banthorpe DV, Hughes ED, Ingold C, Roy J. 652. Mechanism of the benzidine and semidine rearrangements. Part VIII. Some acidity functions in aqueous dioxan. Kinetics of rearrangement of hydrazobenzene at high acidities Journal of the Chemical Society (Resumed). 3294-3299. DOI: 10.1039/Jr9620003294 |
0.691 |
|
1962 |
Banthorpe DV, Hughes ED, Ingold C. 465. Mechanism of benzidine and semidine rearrangements. Part V. Transitional kinetics and products of acid rearrangement of N-1-naphthyl- N′-phenylhydrazine Journal of the Chemical Society (Resumed). 2418-2428. DOI: 10.1039/Jr9620002418 |
0.683 |
|
1962 |
Banthorpe DV, Hughes ED, Ingold C. 461. Mechanism of benzidine and semidine rearrangements. Part I. Kinetic dichotomy: Kinetics, solvent-isotope effect, and products of acid rearrangement of 1,1′-hydrazonaphthalene Journal of the Chemical Society (Resumed). 2386-2401. DOI: 10.1039/Jr9620002386 |
0.719 |
|
1961 |
Charman HB, Hughes ED, Ingold C, Volger HC. 228. Mechanism of electrophilic substitution at a saturated carbon atom. Part V. Kinetics, stereochemistry, and mechanism of anion-catalysed one-alkyl mercury-exchange reactions Journal of the Chemical Society (Resumed). 1142-1151. DOI: 10.1039/Jr9610001142 |
0.844 |
|
1961 |
Charman HB, Hughes ED, Ingold C, Thorpe FG. 226. Mechanism of electrophilic substitution at a saturated carbon atom. Part III. Kinetics, stereochemistry, and mechanism of the three-alkyl mercury-exchange reaction Journal of the Chemical Society (Resumed). 1121-1133. |
0.767 |
|
1961 |
Hughes ED, Volger HC. 459. Mechanism of electrophilic substitution at a saturated carbon atom. Part VI. The pattern of steric effects among alkyl groups and mechanisms in one-alkyl mercury-exchange Journal of the Chemical Society (Resumed). 2359-2365. |
0.829 |
|
1961 |
Hughes ED, Ingold C, Thorpe FG, Volger HC. 227. Mechanism of electrophilic substitution at a saturated carbon atom. Part IV. Kinetics, stereochemistry, and mechanism of the uncatalysed one-alkyl mercury-exchange reaction Journal of the Chemical Society (Resumed). 1133-1142. |
0.847 |
|
1960 |
Hughes ED, Ingold C, Parker AJ. 853. Mechanism of substitution at a saturated carbon atom. Part LXI. Addendum on the Finkelstein reaction, and reply to Farhat-Aziz and Molewyn-Hughes Journal of the Chemical Society (Resumed). 4400-4405. DOI: 10.1039/Jr9600004400 |
0.765 |
|
1960 |
Banthorpe DV, Hughes ED, Ingold C. 799. Mechanism of elimination reactions. Part XX. The inessentiality of steric strain in bimolecular olefin elimination Journal of the Chemical Society (Resumed). 4054-4087. DOI: 10.1039/Jr9600004054 |
0.696 |
|
1960 |
Harvey SH, Hoye PAT, Hughes ED, Ingold C. 163. Reaction kinetics and the Walden inversion. Part VIII. Steric course of bimolecular nucleophilic substitution by an anionic substituting agent in a cationic substrate Journal of the Chemical Society (Resumed). 800-806. DOI: 10.1039/Jr9600000800 |
0.724 |
|
1960 |
Hughes ED, Maynard JC. 800. Mechanism of elimination reactions. Part XXI. Anomalous elimination from αα′-dichlorosuccinic acid Journal of the Chemical Society (Resumed). 4087-4094. |
0.387 |
|
1960 |
Hiron F, Hughes ED. 162. Reaction kinetics and the Walden inversion. Part VII. The configurations of some amino-hydrocarbons Journal of the Chemical Society (Resumed). 795-799. |
0.348 |
|
1960 |
Hughes ED, Whittingham DJ. 164. Mechanism of substitution at a saturated carbon atom. Part LX. Nucleophilic substitutions of the "missing" charge type Journal of the Chemical Society (Resumed). 806-809. |
0.336 |
|
1960 |
Hughes ED, Wilby J. 801. Mechanism of elimination reactions. Part XXII. Anomalous elimination from the trimethylneomenthylammonium ion Journal of the Chemical Society (Resumed). 4094-4101. |
0.315 |
|
1959 |
Backhurst JD, Hughes ED, Ingold C. Homolytic substitution at a saturated carbon atom. Part II. Products of the photoinduced gaseous chlorination of t-butylbenzene Journal of the Chemical Society (Resumed). 2742-2745. DOI: 10.1039/Jr9590002742 |
0.691 |
|
1959 |
Duffin HC, Hughes ED, Ingold C. Homolytic substitution at a saturated carbon atom. Part I. Products of the gaseous nitration of t-butylbenzene Journal of the Chemical Society (Resumed). 2734-2741. DOI: 10.1039/Jr9590002734 |
0.69 |
|
1959 |
Charman HB, Hughes ED, Ingold C. Mechanism of electrophilic substitution at a saturated carbon atom. Part II. Kinetics, stereochemistry, and mechanism of the two-alkyl mercury-exchange reaction Journal of the Chemical Society (Resumed). 2530-2538. DOI: 10.1039/Jr9590002530 |
0.777 |
|
1959 |
Charman HB, Hughes ED, Ingold C. Mechanism of electrophilic substitution at a saturated carbon atom. Part I. Scope and plan. Optical activity from a single asymmetric carbon atom bearing a metal Journal of the Chemical Society (Resumed). 2523-2530. DOI: 10.1039/Jr9590002523 |
0.698 |
|
1958 |
Blackall EL, Hughes ED, Ingold C, Pearson RB. 885. Nitration at nitrogen and oxygen centres. Part II. Kinetics and mechanism of the conversion of alcohols, glycols, and glycerol into their nitric esters Journal of the Chemical Society (Resumed). 4366-4374. DOI: 10.1039/Jr9580004366 |
0.669 |
|
1958 |
Hughes ED, Ingold C, Pearson RB. 884. Nitration at nitrogen and oxygen centres. Part I. Kinetics and mechanism of the conversion of secondary amines into nitroamines Journal of the Chemical Society (Resumed). 4357-4365. DOI: 10.1039/Jr9580004357 |
0.682 |
|
1958 |
Brownstein S, Bunton CA, Hughes ED. 883. The rearrangement of aromatic N-nitroamines. Part II. Isotopic test for intramolecular character in the nitro-transfers from side-chain to ortho- and para-positions Journal of the Chemical Society (Resumed). 4354-4357. DOI: 10.1039/JR9580004354 |
0.421 |
|
1958 |
De La Mare PBD, Hughes ED, Merriman PC, Pichat L, Vernon CA. 519. Kinetics and mechanisms of nucleophilic displacement in allylic systems. Part IX. Bimolecular substitution with rearrangement in the reaction of 1-tert.-butylallyl chloride with ethoxide ion Journal of the Chemical Society (Resumed). 2563-2566. DOI: 10.1039/JR9580002563 |
0.66 |
|
1958 |
Hughes ED, Ingold CK, Ridd JH. 18. Nitrosation, diazotisation, and deamination. Part VI. Comparative discussion of mechanisms of N- and O-nitrosation with special reference to diazotisation Journal of the Chemical Society (Resumed). 88-98. DOI: 10.1039/JR9580000088 |
0.599 |
|
1958 |
Hughes ED, Ingold CK, Ridd JH. 16. Nitrosation, diazotisation, and deamination. Part IV. Hydrogen-ion catalysis in the diazotisation of o-chloroaniline in dilute perchloric acid Journal of the Chemical Society (Resumed). 77-82. DOI: 10.1039/JR9580000077 |
0.619 |
|
1958 |
Hughes ED, Ingold CK, Ridd JH. 14. Nitrosation, diazotisation, and deamination. Part II. Second- and third-order diazotisation of aniline in dilute perchloric acid Journal of the Chemical Society (Resumed). 65-69. DOI: 10.1039/JR9580000065 |
0.614 |
|
1958 |
Hughes ED, Ingold CK, Ridd JH. 13. Nitrosation, diazotisation, and deamination. Part I. Principles, background, and method for the kinetic study of diazotisation Journal of the Chemical Society (Resumed). 58-65. DOI: 10.1039/JR9580000058 |
0.6 |
|
1957 |
Hughes ED, Ingold CK, Patai S, Pocker Y. Mechanism of substitution at a saturated carbon atom. Part LIII. Conductances of some quaternary ammonium salts in benzene, as a preliminary to the study of unimolecular nucleophilic substitution in that solvent Journal of the Chemical Society (Resumed). 1206-1219. |
0.728 |
|
1957 |
Hughes ED, Ingold CK, Mok SF, Patai S, Pocker Y. Mechanism of substitution at a saturated carbon atom. Part LIV. Kinetics of chlorine exchange between triphenylmethyl chloride and tetra-n-butylammonium chloride in benzene Journal of the Chemical Society (Resumed). 1220-1230. |
0.731 |
|
1957 |
Hughes ED, Ingold CK, Patai S, Pocker Y. Mechanism of substitution at a saturated carbon atom. Part LV. Kinetics of the reaction of triphenylmethyl chloride with tetra-n-butylammonium azide in benzene Journal of the Chemical Society (Resumed). 1230-1237. |
0.751 |
|
1957 |
Hughes ED, Ingold CK, Patai S, Pocker Y. Mechanism of substitution at a saturated carbon atom. Part LVII. Kinetics of the reaction of triphenylmethyl chloride with benzyl alcohol in benzene Journal of the Chemical Society (Resumed). 1256-1264. |
0.734 |
|
1957 |
Hughes ED, Ingold CK, Mok SF, Patai S, Pocker Y. Mechanism of substitution at a saturated carbon atom. Part LVIII. Mechanism of sn1 substitutions in a solvent of low solvating power. A comparative discussion Journal of the Chemical Society (Resumed). 1265-1279. |
0.715 |
|
1957 |
Hughes ED, Ingold CK, Mok SF, Pocker Y. Mechanism of substitution at a saturated carbon atom. Part LVI. Kinetics of the reaction of triphenylmethyl chloride with methyl alcohol in benzene Journal of the Chemical Society (Resumed). 1238-1255. |
0.729 |
|
1956 |
De La Mare PBD, Hughes ED. Mechanism of substitution at a saturated carbon atom. part l.* kinetic effects of phenyl and halogen substituents in alkyl halides on their reactions with halide ions in acetone Journal of the Chemical Society (Resumed). 835-839. |
0.434 |
|
1956 |
Charlton JC, Hughes ED. Mechanism of substitution at a saturated carbon atom. part li i* polar and steric ortho-effects in bimolecular finkelstein substitutions of arylalkyl halides Journal of the Chemical Society (Resumed). 845-849. |
0.36 |
|
1956 |
Charlton JC, Hughes ED. Mechanism of substitution at a saturated carbon atom. part li.* ortho-effects in solvolysis of arylalkyl halides, illustrating steric retardation in a unimolecular substitution Journal of the Chemical Society (Resumed). 840-845. |
0.393 |
|
1955 |
De La Mare PBD, Fowden L, Hughes ED, Ingold CK, Mackie JDH. Mechanism of substitution at a saturated carbon atom. Part XLIX. Analysis of steric and polar effects of alkyl groups in bimolecular nucleophilic substitution, with special reference to halogen exchanges Journal of the Chemical Society (Resumed). 3200-3236. DOI: 10.1039/JR9550003200 |
0.71 |
|
1955 |
Fowden L, Hughes ED, Ingold CK. Mechanism of substitution at a saturated carbon atom. Part XLVII. Kinetics of the interaction of bromide ions with simple alkyl iodides in acetone Journal of the Chemical Society (Resumed). 3193-3196. DOI: 10.1039/JR9550003193 |
0.717 |
|
1955 |
Fowden L, Hughes ED, Ingold CK. Mechanism of substitution at a saturated carbon atom. Part XLVI. Kinetics of the interaction of iodide ions with simple alkyl bromides in acetone Journal of the Chemical Society (Resumed). 3187-3192. DOI: 10.1039/JR9550003187 |
0.717 |
|
1955 |
Hughes ED, Ingold CK, Mackie JDH. Mechanism of substitution at a saturated carbon atom. Part XLIV. Kinetics of the interaction of iodide ions with simple alkyl chlorides in acetone Journal of the Chemical Society (Resumed). 3177-3179. DOI: 10.1039/JR9550003177 |
0.718 |
|
1955 |
Hughes ED, Ingold CK, Mackie JDH. Mechanism of substitution at a saturated carbon atom. Part XLIII. Kinetics of the interaction of chloride ions with simple alkyl bromides in acetone Journal of the Chemical Society (Resumed). 3173-3177. DOI: 10.1039/JR9550003173 |
0.719 |
|
1954 |
Charlton JC, Hughes ED. Mechanism of substitution at a saturated carbon atom. Part XLI. Unimolecular racemisation of l-mesitylethyl chloride in acetone Journal of the Chemical Society (Resumed). 2939-2942. DOI: 10.1039/JR9540002939 |
0.323 |
|
1954 |
De La Mare PBD, Hughes ED, Iingold CK, Pocker Y. Mechanism of substitution at a saturated carbon atom. Part XL. Unimolecular nucleophilic substitution and elimination of tert.-butyl bromide with anionic reagents in nitromethane solvent; With some remarks on the addition of acids to olefins Journal of the Chemical Society (Resumed). 2930-2939. DOI: 10.1039/JR9540002930 |
0.448 |
|
1954 |
Gelles E, Hughes ED, Ingold CK. Mechanism of substitution at a saturated carbon atom. Part XXXIX. Nucleophilic substitutions in tertiary alkyl halides by hydroxylic reagents in nitromethane solvent Journal of the Chemical Society (Resumed). 2918-2929. DOI: 10.1039/JR9540002918 |
0.739 |
|
1954 |
Bunton CA, Greenstreet CH, Hughes ED, Ingold CK. Mechanism of substitution at a saturated carbon atom. Part XXXVIII. Menschutkin reactions of some simple alkyl halides in sulphur dioxide solution Journal of the Chemical Society (Resumed). 647-651. DOI: 10.1039/JR9540000647 |
0.781 |
|
1954 |
Bunton CA, Greenstreet CH, Hughes ED, Ingold CK. Mechanism of substitution at a saturated carbon atom. Part XXXVII. Halide-ion exchange with a simple alkyl halide in sulphur dioxide solution Journal of the Chemical Society (Resumed). 642-646. DOI: 10.1039/JR9540000642 |
0.756 |
|
1954 |
Bird ML, Hughes ED, Ingold CK. Mechanism of substitution at a saturated carbon atom. Part XXXVI. Unimolecular menschutkin reactions in sulphur dioxide solution. Remarks on the theory of border-line mechanisms Journal of the Chemical Society (Resumed). 634-642. DOI: 10.1039/Jr9540000634 |
0.746 |
|
1953 |
Bevan CWL, Hughes ED, Ingold CK. Effects of Alkyl Groups in Nucleophilic Substitution Nature. 171: 301-302. DOI: 10.1038/171301a0 |
0.637 |
|
1953 |
Hughes ED, Ingold CK, Rose JB. Mechanism of elimination reactions. Part XIX. Kinetics and steric course of elimination from isomeric menthyl chlorides Journal of the Chemical Society (Resumed). 3839-3845. |
0.72 |
|
1953 |
Hughes ED, Ingold CK, Pasternak R. Mechanism of elimination reactions. Part XVIII. Kinetics and steric course of elimination from isomeric benzene hexachlorides Journal of the Chemical Society (Resumed). 3832-3839. |
0.716 |
|
1953 |
Hughes ED, Ingold CK, Shiner VJ. Mechanism of elimination reactions. Part XVII. The comparative unimportance of steric strain in unimolecular olefin elimination Journal of the Chemical Society (Resumed). 3827-3832. |
0.671 |
|
1952 |
Blackall EL, Hughes ED, Ingold CK. Kinetics and mechanism of aromatic nitration. Part IX.* Nitrosating agents in nitrations catalysed by nitrous acid Journal of the Chemical Society (Resumed). 28-32. DOI: 10.1039/Jr9520000028 |
0.679 |
|
1952 |
De La Mare PBD, Hughes ED, Vernon CA. Bimolecular Nucleophilic Substitution with Anionotropic Rearrangement Nature. 169: 672-673. DOI: 10.1038/169672b0 |
0.625 |
|
1952 |
Heller HE, Hughes ED, Ingold CK. A new view of the arylhydroxylamine rearrangement Nature. 169: 80. DOI: 10.1038/169080b0 |
0.574 |
|
1952 |
Hawdon AR, Hughes ED, Ingold CK. Mechanism of Substitution at a Saturated Carbon Atom. Part XXXV.* Effect of Temperature on the Competition between Unimolecular Solvolytic and Non-solvolytic Substitutions of Di-p-tolylmethyl Chloride. Activation in the Fast Step of Unimolecular Nonsolvolytic Substitution Journal of the Chemical Society (Resumed). 2479-2487. |
0.702 |
|
1952 |
Benfey OT, Hughes ED, Ingold CK. Mechanism of Substitution at a Saturated Carbon Atom. Part XXXIII.* Kinetic Effect of Common-ion and of Non-common-ion Salts on the Aqueous Solvolysis of Diplienylmethyl Halides. A Demonstration of the Unimolecular Mechanism of Solvolysis Journal of the Chemical Society (Resumed). 2448. |
0.703 |
|
1952 |
Austin AT, Hughes ED, Ingold CK, Ridd JH. Reactions of nitrous acid Journal of the American Chemical Society. 74: 555-556. |
0.692 |
|
1952 |
Hughes ED, Ingold CK. Aromatic rearrangements Quarterly Reviews, Chemical Society. 6: 34-62. |
0.659 |
|
1952 |
Benfey OT, Hughes ED, Ingold CK. Mechanism of Substitution at a Saturated Carbon Atom. Part XXXIV.* Kinetic Effects of Hydroxide and Alkoxide Ions on the Rate-controlling and Product-forming Stages of Unimolecular Solvolysis of tert. -Butyl and Diphenylmethyl Halides Journal of the Chemical Society (Resumed). 2449-2478. |
0.705 |
|
1951 |
Brown F, Hughes ED, Ingold CK, Smith JF. Wagner changes, synartetic acceleration and synartetic ions Nature. 168: 65-67. DOI: 10.1038/168065a0 |
0.584 |
|
1950 |
BREWSTER P, HIRON F, HUGHES ED, INGOLD CK, RAO PA. Configurations of amino-compounds and the steric course of deamination. Nature. 166: 179-80. PMID 15439210 DOI: 10.1038/166179a0 |
0.599 |
|
1950 |
BREWSTER P, HUGHES ED, INGOLD CK, RAO PA. Configuration of carbohydrates, hydroxy-acids and amino-acids; stereochemical standards of configuration. Nature. 166: 178-9. PMID 15439209 |
0.615 |
|
1950 |
DE LA MARE PB, HUGHES ED, VERNON CA. Reaction of chlorine cations with olefins. Research; a Journal of Science and Its Applications. 3: 242-3. PMID 15430636 |
0.646 |
|
1950 |
BUNTON CA, HUGHES ED, INGOLD CK, MEIGH DF. Walden inversion in the acid hydrolysis of carboxylic esters by unimolecular alkyl fission. Nature. 166: 680. PMID 14780195 |
0.702 |
|
1950 |
HUGHES ED, INGOLD CK, MARTIN RJ, MEIGH DF. Walden inversion in unimolecular reactions of secondary and tertiary alkyl halides. Nature. 166: 679-80. PMID 14780194 DOI: 10.1038/166679a0 |
0.695 |
|
1950 |
HUGHES ED, INGOLD CK, RIDD JH. Kinetics and mechanism of diazotization. Nature. 166: 642-3. PMID 14780180 DOI: 10.1038/166642a0 |
0.675 |
|
1950 |
Bunton CA, Hughes ED, Ingold CK, Meigh DF. Walden inversion and reaction mechanism: Walden inversion in the acid hydrolysis of carboxylic esters by unimolecular alkyl fission Nature. 166: 680. DOI: 10.1038/166680a0 |
0.724 |
|
1950 |
Brewster P, Hiron F, Hughes ED, Ingold CK, Rao PADS. Configuration of carbohydrates, hydroxy-acids and amino-acids: Stereochemical standards of configuration Nature. 166: 178-179. DOI: 10.1038/166178a0 |
0.615 |
|
1950 |
Halberstadt ES, Hughes ED, Ingold CK. Kinetics and mechanism of aromatic nitration. Part III. Nitration in acidified aqueous nitric acid Journal of the Chemical Society (Resumed). 2441-2452. |
0.689 |
|
1950 |
Gillespie RJ, Hughes ED, Ingold CK. Cryoscopic measurements in nitric acid. Part I. The solutes dinitrogen pentoxide and water. The self-dissociation of nitric acid Journal of the Chemical Society (Resumed). 2552-2558. |
0.612 |
|
1950 |
Hughes ED, Ingold CK. Mechanism of the benzidine rearrangement Journal of the Chemical Society (Resumed). 1638-1639. |
0.671 |
|
1950 |
Gillespie RJ, Graham J, Hughes ED, Ingold CK, Peeling ERA. Cryoscopic measurements in sulphuric acid. Part III. The solutes nitric acid, dinitrogen pentoxide, dinitrogen tetroxide, and dinitrogen trioxide. Cryoscopic proof of the formation of the nitronium ion, NO2 + Journal of the Chemical Society (Resumed). 2504-2515. |
0.637 |
|
1950 |
Bunton CA, Hughes ED, Ingold CK, Jacobs DIH, Jones MH, Minkoff GJ, Reed RI. Kinetics and mechanism of aromatic nitration. Part VI. The nitration of phenols and phenolic ethers: The concomitant dealkylation of phenolic ethers. The role of nitrous acid Journal of the Chemical Society (Resumed). 2628-2656. |
0.688 |
|
1950 |
Gold V, Hughes ED, Ingold CK. Kinetics and mechanism of aromatic nitration. Part V. Nitration by acyl nitrates, particularly by benzoyl nitrate Journal of the Chemical Society (Resumed). 2467-2473. |
0.669 |
|
1950 |
Hughes ED, Ingold CK, Reed RI. Kinetics and mechanism of aromatic nitration. Part II. Nitration by the nitronium ion, NO2 +, derived from nitric acid Journal of the Chemical Society (Resumed). 2400-2440. |
0.668 |
|
1950 |
Gillespie RJ, Hughes ED, Ingold CK. Cryoscopic measurements in sulphuric acid. Part I. Principles and methods. The cryoscopic constant and some other constants of sulphuric acid Journal of the Chemical Society (Resumed). 2473-2492. |
0.623 |
|
1950 |
Glazer J, Hughes ED, Ingold CK, James AT, Jones GT, Roberts E. Kinetics and mechanism of aromatic nitration. Part VII. Products of nitration of aniline derivatives, especially of dimethylaniline. The concomitant dealkylation of dialkylanilines Journal of the Chemical Society (Resumed). 2657-2678. |
0.667 |
|
1950 |
Gold V, Hughes ED, Ingold CK, Williams GH. Kinetics and mechanism of aromatic nitration. Part IV. Nitration by dinitrogen pentoxide in aprotic solvents Journal of the Chemical Society (Resumed). 2452-2466. |
0.697 |
|
1950 |
Goddard DR, Hughes ED, Ingold CK. Chemistry of nitronium salts. Part I. Isolation of some nitronium salts Journal of the Chemical Society (Resumed). 2559-2575. |
0.592 |
|
1949 |
GILLESPIE RJ, HUGHES ED. Kinetics and mechanism of aromatic nitration. Nature. 163: 599. PMID 18224956 |
0.575 |
|
1948 |
Dhar ML, Hughes ED, Ingold CK, Mandour AMM, Maw GA, Woolf LI. 426. Mechanism of elimination reactions. Part XVI. Constitutional influences in elimination. A general discussion Journal of the Chemical Society (Resumed). 2093-2119. DOI: 10.1039/Jr9480002093 |
0.72 |
|
1948 |
Hughes ED, Ingold CK, Maw GA. 422. Mechanism of elimination reactions. Part XII. Kinetics of olefin eliminations from ethyl-, n-propyl-, n-butyl, isobutyl-, and 2-phenyl-ethyl-dimethylsulphonium salts in alkaline alcoholic media Journal of the Chemical Society (Resumed). 2072-2077. DOI: 10.1039/Jr9480002072 |
0.698 |
|
1948 |
Dhar ML, Hughes ED, Ingold CK. 421. Mechanism of elimination reactions. Part XI. Kinetics of olefin elimination from tert.-butyl and tert.-amyl bromides in acidic and alkalinc alcoholic media Journal of the Chemical Society (Resumed). 2065-2072. DOI: 10.1039/Jr9480002065 |
0.723 |
|
1948 |
Dhar ML, Hughes ED, Ingold CK. 420. Mechanism of elimination reactions. Part X. Kinetics of olefin elimination from isopropyl, sec.-butyl, 2-n-amyl, and 3-n-amyl bromides in acidic and alkaline alcoholic media Journal of the Chemical Society (Resumed). 2058-2065. DOI: 10.1039/Jr9480002058 |
0.699 |
|
1948 |
Dhar ML, Hughes ED, Ingold CK, Masterman S. 419. Mechanism of elimination reactions. Part IX. Kinetics of olefin elimination from n-propyl, n-butyl, n-amyl, and isobutyl bromides in alkaline alcoholic media Journal of the Chemical Society (Resumed). 2055-2057. DOI: 10.1039/Jr9480002055 |
0.677 |
|
1948 |
Cooper KA, Dhar ML, Hughes ED, Ingold CK, MacNulty BJ, Woolf LI. 417. Mechanism of elimination reactions. Part VII. Solvent effects on rates and product-proportions in uni- and bi-molecular substitution and elimination reactions of alkyl halides and sulphonium salts in hydroxylic solvents Journal of the Chemical Society (Resumed). 2043-2049. DOI: 10.1039/Jr9480002043 |
0.738 |
|
1948 |
Cooper KA, Hughes ED, Ingold CK, MacNulty BJ. 416. Mechanism of elimination reactions. Part VI. Introduction to a group of papers. Unimolecular olefin formation from tert.-butyl- and tert.-amyl-sulphonium salts Journal of the Chemical Society (Resumed). 2038-2042. DOI: 10.1039/Jr9480002038 |
0.724 |
|
1948 |
Gripenberg J, Hughes ED, Ingold CK. Effect of ionic charges on the energy and entropy of activation of heterolytic reactions [11] Nature. 161: 480-481. |
0.628 |
|
1947 |
HUGHES ED, INGOLD CK, EVANS AG. Reactions of organic halides in solution. Nature. 159: 166. PMID 20285653 |
0.655 |
|
1947 |
DOSTROVSKY I, HUGHES ED, INGOLD CK. neoPentyl Alcohol and Steric Hindrance Nature. 160: 901-902. DOI: 10.1038/160901B0 |
0.623 |
|
1947 |
AUSTIN AT, HUGHES ED, INGOLD CK. Text-book Organic Chemistry Nature. 160: 406-406. DOI: 10.1038/160406C0 |
0.577 |
|
1946 |
HUGHES ED, INGOLD CK, REED RI. Kinetics of aromatic nitration; the nitronium ion. Nature. 158: 448. PMID 20999103 DOI: 10.1038/158448C0 |
0.629 |
|
1946 |
HUGHES ED, INGOLD CK. Reactions of organic halides in solution. Nature. 158: 94. PMID 20993334 DOI: 10.1038/158094B0 |
0.715 |
|
1946 |
HALBERSTADT ES, HUGHES ED, INGOLD CK. Kinetics of Aromatic Nitration : the Nitracidium Ion Nature. 158: 514-514. DOI: 10.1038/158514b0 |
0.624 |
|
1946 |
GODDARD DR, HUGHES ED, INGOLD CK. Isolation of Salts of the Nitronium Ion Nature. 158: 480-480. DOI: 10.1038/158480B0 |
0.627 |
|
1945 |
Benford GA, Bunton CA, Halberstadt ES, Hughes ED, Ingold CK, Minkoff GJ, Reed RI. Univalent electron transfers in aromatic nitration? [1] Nature. 156: 688. |
0.58 |
|
1944 |
Bateman LC, Hughes ED, Ingold CK. Molecular compounds between amines and sulphur dioxide. A comment on Jander's theory of ionic reactions in sulphur dioxide Journal of the Chemical Society (Resumed). 243-247. DOI: 10.1039/Jr9440000243 |
0.692 |
|
1943 |
Bird ML, Hughes ED, Ingold CK. A criterion for the mechanism of the reaction between alkyl halides and hydroxylic solvents. Part III. Reactions of n-butyl bromide Journal of the Chemical Society (Resumed). 255-261. DOI: 10.1039/Jr9430000255 |
0.736 |
|
1941 |
Dhar ML, Mandour AMM, Hughes ED, Webb FR, Ingold CK, Woolf LI. Elimination reactions in organic chemistry Nature. 147: 812-813. DOI: 10.1038/147812A0 |
0.662 |
|
1941 |
Hughes ED, Ingold CK, Whitfield IC. The walden inversion in the replacement of hydroxyl by halogen [3] Nature. 147: 206-207. |
0.618 |
|
1940 |
Bateman LC, Hughes ED, Ingold CK. Mechanism of substitution at a saturated carbon atom. Part XXV. Unimolecular halogen exchange between an alkyl halide and halide ions in sulphur dioxide solution; and a concluding note Journal of the Chemical Society (Resumed). 1017-1029. DOI: 10.1039/Jr9400001017 |
0.736 |
|
1940 |
Bateman LC, Hughes ED, Ingold CK. Mechanism of substitution at a saturated carbon atom. Part XXIV. Qualitative survey of nucleophilic substitutions of benzhydryl halides in sulphur dioxide solution Journal of the Chemical Society (Resumed). 1011-1017. DOI: 10.1039/Jr9400001011 |
0.736 |
|
1940 |
Bateman LC, Church MG, Hughes ED, Ingold CK, Taher NA. Mechanism of substitution at a saturated carbon atom. Part XXIII. A kinetic demonstration of the unimolecular solvolysis of alkyl halides. (Section E) a general discussion Journal of the Chemical Society (Resumed). 979-1011. DOI: 10.1039/Jr9400000979 |
0.728 |
|
1940 |
Bateman LC, Hughes ED, Ingold CK. Mechanism of substitution at a saturated carbon atom. Part XIX. A kinetic demonstration of the unimolecular solvolysis of alkyl halides. (Section A) kinetics of, and salt effects in, the hydrolysis of tert.-butyl bromide in aqueous acetone Journal of the Chemical Society (Resumed). 960-966. DOI: 10.1039/Jr9400000960 |
0.764 |
|
1940 |
Hughes ED, Taher NA. 183. Mechanism of substitution at a saturated carbon atom. Part XVIII. Polar effect of the carboxylate ion group as illustrated by the hydrolysis of the bromomalonate and α-bromomethylmalonate ions Journal of the Chemical Society (Resumed). 956-960. DOI: 10.1039/Jr9400000956 |
0.407 |
|
1940 |
Hughes ED, Ingold CK, Taher NA. Mechanism of substitution at a saturated carbon atom. Part XVII. Polar effects in alkyl groups, as illustrated by solvolytic substitutions of p-alkylbenzhydryl chlorides Journal of the Chemical Society (Resumed). 949-956. DOI: 10.1039/Jr9400000949 |
0.721 |
|
1940 |
Bateman LC, Hughes ED. 181. Mechanism of substitution at a saturated carbon atom. Part XVI. Hydrolysis of methyl, ethyl, isopropyl and tert.-butyl bromides in acidic solutions under conditions believed to be conducive to uniformity of mechanism Journal of the Chemical Society (Resumed). 945-948. DOI: 10.1039/Jr9400000945 |
0.49 |
|
1940 |
Bateman LC, Hughes ED. 180. Mechanism of substitution at a saturated carbon atom. Part XV. Unimolecular and bimolecular substitutions of n-butyl bromide with water, and with anions, as substituting agents in formic acid solution Journal of the Chemical Society (Resumed). 940-944. DOI: 10.1039/Jr9400000940 |
0.481 |
|
1940 |
Bateman LC, Hughes ED. 179. Mechanism of substitution at a saturated carbon atom. Part XIV. Unimolecular substitutions of tert.-butyl chloride with water, and with anions, as substituting agents in formic acid solution Journal of the Chemical Society (Resumed). 935-940. DOI: 10.1039/Jr9400000935 |
0.485 |
|
1940 |
Bateman LC, Cooper KA, Hughes ED, Ingold CK. Mechanism of substitution at a saturated carbon atom. Part XIII. Mechanisms operative in the hydrolysis of methyl, ethyl, isopropyl, and tert.-butyl bromides in aqueous solutions Journal of the Chemical Society (Resumed). 925-935. DOI: 10.1039/Jr9400000925 |
0.73 |
|
1940 |
Church MG, Hughes ED. 177. Mechanism of substitution at a saturated carbon atom. Part XII. Hydrolysis of benzhydryl chloride in acidic moist acetone Journal of the Chemical Society (Resumed). 920-925. DOI: 10.1039/Jr9400000920 |
0.501 |
|
1940 |
Bateman LC, Cooper KA, Hughes ED. 176. Mechanism of substitution at a saturated carbon atom. Part XI. Hydrolysis of tert.-butyl bromide in acidic moist acetone Journal of the Chemical Society (Resumed). 913-920. DOI: 10.1039/Jr9400000913 |
0.506 |
|
1940 |
Hughes ED, Ingold CK, Masterman S, McNulty BJ. Mechanism of elimination reactions. Part V. Kinetics of olefin elimination from ethyl, isopropyl, tert.-butyl and α- and β-phenylethyl bromides in acidic and in alkaline alcoholic solution. Effects due to, and factors influencing, the two mechanisms of elimination Journal of the Chemical Society (Resumed). 899-912. DOI: 10.1039/Jr9400000899 |
0.712 |
|
1939 |
Hughes ED, Ingold CK, Masterman S. 179. Ancillary mechanisms in the hydrolysis and esterification of carboxylic esters Journal of the Chemical Society (Resumed). 840-842. DOI: 10.1039/Jr9390000840 |
0.715 |
|
1938 |
Bateman LC, Hughes ED, Ingold CK. 171. A criterion for the mechanism of the reaction between alkyl halides and hydroxylic solvents. Reactions of tert.-butyl chloride Journal of the Chemical Society (Resumed). 881-887. DOI: 10.1039/Jr9380000881 |
0.742 |
|
1938 |
Cowdrey WA, Hughes ED, Nevell TP, Wilson CL. 39. Aliphatic substitution and the Walden inversion. Part III. Comparison, using radioactive bromine, of the rates of inversion and substitution in the reaction of bromide ions with α-bromopropionic acid Journal of the Chemical Society (Resumed). 209-211. DOI: 10.1039/Jr9380000209 |
0.439 |
|
1938 |
Bateman LC, Hughes ED, Ingold CK. A criterion for the mechanism of the reactions of alkyl halides with hydroxylic solvents. Reactions of benzhydryl chloride Journal of the American Chemical Society. 60: 3080-3082. DOI: 10.1021/Ja01279A501 |
0.74 |
|
1937 |
Hughes ED, MacNulty BJ. 261. The mechanism of elimination reactions. Part IV. Unimolecular olefin formation from tert.-amyl halides in acid and alkaline aqueous solutions, and some remarks on the scope of the unimolecular mechanism Journal of the Chemical Society (Resumed). 1283-1291. DOI: 10.1039/Jr9370001283 |
0.497 |
|
1937 |
Cooper KA, Hughes ED, Ingold CK. The mechanism of elimination reactions. Part III. Unimolecular olefin formation from tert.-butyl halides in acid and alkaline aqueous solutions Journal of the Chemical Society (Resumed). 1280-1283. DOI: 10.1039/Jr9370001280 |
0.737 |
|
1937 |
Hughes ED, Ingold CK, Shapiro UG. The mechanism of elimination reactions. Part II. Unimolecular olefin formation from sec.-octyl halides in aqueous alcohol. A new criterion of mechanism Journal of the Chemical Society (Resumed). 1277-1280. DOI: 10.1039/Jr9370001277 |
0.714 |
|
1937 |
Hughes ED, Ingold CK, Scott AD. The mechanism of elimination reactions. Part I. Unimolecular olefin formation from alkyl halides in sulphur dioxide and formic acid Journal of the Chemical Society (Resumed). 1271-1277. DOI: 10.1039/Jr9370001271 |
0.759 |
|
1937 |
Cowdrey WA, Hughes ED, Ingold CK, Masterman S, Scott AD. Reaction kinetics and the Walden inversion. Part VI. Relation of steric orientation to mechanism in substitutions involving halogen atoms and simple or substituted hydroxyl groups Journal of the Chemical Society (Resumed). 1252-1271. DOI: 10.1039/Jr9370001252 |
0.752 |
|
1937 |
Cowdrey WA, Hughes ED, Ingold CK. Reaction kinetics and the Walden inversion. Part V. Action of silver salts in hydroxylic solvents on α-bromopropionic acid, its methyl ester, and sodium salt Journal of the Chemical Society (Resumed). 1243-1252. DOI: 10.1039/Jr9370001243 |
0.719 |
|
1937 |
Hughes ED, Ingold CK, Masterman S. Reaction kinetics and the Walden inversion. Part IV. Action of silver salts in hydroxylic solvents on β-n-octyl bromide and α-phenylethyl chloride Journal of the Chemical Society (Resumed). 1236-1243. DOI: 10.1039/Jr9370001236 |
0.693 |
|
1937 |
Cowdrey WA, Hughes ED, Ingold CK. Reaction kinetics and the Walden inversion. Part III. Homogeneous hydrolysis and alcoholysis of α-bromopropionic acid, its ester and anion Journal of the Chemical Society (Resumed). 1208-1236. DOI: 10.1039/Jr9370001208 |
0.716 |
|
1937 |
Hughes ED, Ingold CK, Scott AD. Reaction kinetics and the Walden inversion. Part II. Homogeneous hydrolysis, alcoholysis, and ammonolysis of α-phenylethyl halides Journal of the Chemical Society (Resumed). 1201-1208. DOI: 10.1039/Jr9370001201 |
0.693 |
|
1937 |
Hughes ED, Ingold CK, Masterman S. Reaction kinetics and the Walden inversion. Part I. Homogeneous hydrolysis and alcoholysis of β-n-octyl halides Journal of the Chemical Society (Resumed). 1196-1201. DOI: 10.1039/Jr9370001196 |
0.683 |
|
1937 |
Hughes ED, Shapiro UG. 251. Mechanism of substitution at a saturated carbon atom. Part X. Hydrolysis of β-n-octyl bromide Journal of the Chemical Society (Resumed). 1192-1196. DOI: 10.1039/Jr9370001192 |
0.411 |
|
1937 |
Bateman LC, Hughes ED. 250. Mechanism of substitution at a saturated carbon atom. Part IX. The rôle of the solvent in the first-order hydrolysis of alkyl halides Journal of the Chemical Society (Resumed). 1187-1192. DOI: 10.1039/Jr9370001187 |
0.494 |
|
1937 |
Cooper KA, Hughes ED. 249. Mechanism of substitution at a saturated carbon atom. Part VIII. Hydrolysis of tert.-butyl halides Journal of the Chemical Society (Resumed). 1183-1187. DOI: 10.1039/Jr9370001183 |
0.489 |
|
1937 |
Hughes ED, Shapiro UG. 248. Mechanism of substitution at a saturated carbon atom. Part VII. Hydrolysis of isopropyl halides Journal of the Chemical Society (Resumed). 1177-1183. DOI: 10.1039/Jr9370001177 |
0.481 |
|
1936 |
Hughes ED, Ingold CK, Shapiro UG. Mechanism of substitution at a saturated carbon atom. Part VI. Hydrolysis of isopropyl bromide Journal of the Chemical Society (Resumed). 225-236. DOI: 10.1039/Jr9360000225 |
0.739 |
|
1936 |
COWDREY WA, HUGHES ED, INGOLD CK. Reaction Kinetics and the Walden Inversion Nature. 138: 759-759. DOI: 10.1038/138759A0 |
0.681 |
|
1936 |
Hughes ED, Ingold CK, Scott AD. Unimolecular elimination and the significance of the electrical conduction, racemization and halogen replacement of organic halides in solution [2] Nature. 138: 120-121. DOI: 10.1038/138120B0 |
0.629 |
|
1935 |
Hughes ED. 56. Mechanism of substitution at a saturated carbon atom. Part V. Hydrolysis of tert.-butyl chloride Journal of the Chemical Society (Resumed). 255-258. DOI: 10.1039/Jr9350000255 |
0.482 |
|
1935 |
Hughes ED, Ingold CK. Mechanism of substitution at a saturated carbon atom. Part IV. A discussion of constitutional and solvent effects on the mechanism, kinetics, velocity, and orientation of substitution Journal of the Chemical Society (Resumed). 244-255. DOI: 10.1039/Jr9350000244 |
0.752 |
|
1935 |
Gleave JL, Hughes ED, Ingold CK. Mechanism of substitution at a saturated carbon atom. Part III. Kinetics of the degradations of sulphonium compounds Journal of the Chemical Society (Resumed). 236-244. DOI: 10.1039/Jr9350000236 |
0.73 |
|
1934 |
Day JNE, Hughes ED, Ingold CK, Wilson CL. 349. Hydration of salts with heavy water, and remarks on the constitution of salt hydrates Journal of the Chemical Society (Resumed). 1593-1599. DOI: 10.1039/Jr9340001593 |
0.62 |
|
1934 |
Hughes ED, Ingold CK, Wilson CL. 112. Separation of the isotopes of hydrogen by the chemical decomposition of water, and some remarks on the mechanisms underlying the reducing action of dissolving metals Journal of the Chemical Society (Resumed). 493-498. DOI: 10.1039/Jr9340000493 |
0.65 |
|
1934 |
HUGHES ED, INGOLD CK, WILSON CL. Concentration of Heavy Water by Spontaneous Evaporation Nature. 134: 142-142. DOI: 10.1038/134142A0 |
0.584 |
|
1934 |
HUGHES ED, INGOLD CK, WILSON CL. Chemical Separation of the Isotopes of Hydrogen Nature. 133: 291-292. DOI: 10.1038/133291A0 |
0.599 |
|
1933 |
HUGHES ED, INGOLD CK. Dynamics and Mechanism of Aliphatic Substitutions Nature. 132: 933-934. DOI: 10.1038/132933B0 |
0.667 |
|
1930 |
Hughes ED, Watson HB. CCXXVI.—The reaction of bromine with aliphatic acids. Part IV. Succinic acid Journal of the Chemical Society (Resumed). 1733-1740. DOI: 10.1039/Jr9300001733 |
0.403 |
|
1929 |
Hughes ED, Watson HB. CCLV.—The reaction of bromine with aliphatic acids. Part III. α-and γ-Ketonic acids Journal of the Chemical Society (Resumed). 1945-1954. DOI: 10.1039/Jr9290001945 |
0.394 |
|
Show low-probability matches. |