Kenneth Schofield

466 total citations
30 papers, 308 citations indexed

About

Kenneth Schofield is a scholar working on Organic Chemistry, Physical and Theoretical Chemistry and Spectroscopy. According to data from OpenAlex, Kenneth Schofield has authored 30 papers receiving a total of 308 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Organic Chemistry, 13 papers in Physical and Theoretical Chemistry and 12 papers in Spectroscopy. Recurrent topics in Kenneth Schofield's work include Chemical Reaction Mechanisms (26 papers), Chemical Reactions and Mechanisms (13 papers) and Organic and Inorganic Chemical Reactions (12 papers). Kenneth Schofield is often cited by papers focused on Chemical Reaction Mechanisms (26 papers), Chemical Reactions and Mechanisms (13 papers) and Organic and Inorganic Chemical Reactions (12 papers). Kenneth Schofield collaborates with scholars based in . Kenneth Schofield's co-authors include Roy B. Moodie, M. R. Grimmett, Ian J. Ferguson, John B. Weston, James W. Barnett, Peter G. Taylor, R. G. Coombes, Lyndsay Main, Paul Rys and Tadao Yoshida and has published in prestigious journals such as Accounts of Chemical Research, Journal of the Chemical Society Perkin Transactions 1 and Journal of the Chemical Society Chemical Communications.

In The Last Decade

Kenneth Schofield

26 papers receiving 285 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Kenneth Schofield	10	220	46	40	39	31	30	308
Peter V. Alston United States	13	322 1.5×	26 0.6×	35 0.9×	44 1.1×	49 1.6×	28	425
M. K. Hargreaves United Kingdom	7	230 1.0×	30 0.7×	57 1.4×	95 2.4×	17 0.5×	34	344
Wilson B. Lutz United States	7	225 1.0×	76 1.7×	99 2.5×	69 1.8×	17 0.5×	15	318
Uwe M. Oehler Canada	7	178 0.8×	86 1.9×	22 0.6×	29 0.7×	15 0.5×	12	349
Leallyn B. Clapp United States	12	298 1.4×	27 0.6×	30 0.8×	104 2.7×	25 0.8×	53	399
Richard Baltzly United Kingdom	10	213 1.0×	26 0.6×	40 1.0×	70 1.8×	21 0.7×	33	298
Sylvia H. Flood	10	277 1.3×	61 1.3×	54 1.4×	26 0.7×	31 1.0×	11	389
M. V. GEORGE India	10	244 1.1×	71 1.5×	19 0.5×	38 1.0×	22 0.7×	27	310
Robert O. Kan United States	10	257 1.2×	51 1.1×	37 0.9×	72 1.8×	18 0.6×	11	344
Edward R. Atkinson United States	11	192 0.9×	42 0.9×	33 0.8×	91 2.3×	8 0.3×	32	366

Countries citing papers authored by Kenneth Schofield

Since Specialization

Citations

This map shows the geographic impact of Kenneth Schofield's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Kenneth Schofield with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kenneth Schofield more than expected).

Fields of papers citing papers by Kenneth Schofield

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kenneth Schofield. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Kenneth Schofield. The network helps show where Kenneth Schofield may publish in the future.

Co-authorship network of co-authors of Kenneth Schofield

This figure shows the co-authorship network connecting the top 25 collaborators of Kenneth Schofield. A scholar is included among the top collaborators of Kenneth Schofield based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Kenneth Schofield. Kenneth Schofield is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Moodie, Roy B., et al.. (1988). Electrophilic aromatic substitution. Part 34. Nitration of 1-chloro-4-nitro-benzene, 1,3-dichloro-2-nitrobenzene, 1,3-dinitrobenzene, 1-chloro-2,4-dinitro-benzene, and 2-chloro-1,3-dinitrobenzene in sulphuric acid and oleum. Journal of the Chemical Society Perkin Transactions 2. 1637–1637. 2 indexed citations

Moodie, Roy B., et al.. (1985). Electrophilic aromatic substitution. Part 32. The nitration of 1,3,5-trichloro-2-nitrobenzene, 1,3,5-trichloro-2,6-dinitrobenzene, and 1,2,3,5-tetrachloro-4,6-dinitrobenzene in sulphuric acid and in oleum. Journal of the Chemical Society Perkin Transactions 2. 1457–1457.

Moodie, Roy B., et al.. (1984). Electrophilic aromatic substitution. Part 31. The kinetics and products of nitration of naphthalene, biphenyl, and some reactive monocyclic aromatic substrates in aqueous phosphoric acid containing nitric acid or propyl nitrate. Journal of the Chemical Society Perkin Transactions 2. 921–921. 2 indexed citations

Moodie, Roy B., et al.. (1983). Nitration of 1,3,5-trichloro-2,4-dinitrobenzene: nitro-denitration. Journal of the Chemical Society Chemical Communications. 233–233.

Bloomfield, C., Roy B. Moodie, & Kenneth Schofield. (1983). Electrophilic aromatic substitution. Part 29. The kinetics and products of the solvolyses in aqueous sulphuric acids of 2-cyano-3,4-dimethyl-4-nitrocyclohexa-2,5-dienyl acetate: the non-occurrence of an intramolecular 1,3-migration of the nitro-group in the solvolytic reactions of the diene. The kinetics and products of nitration of 2,3-and 3,4-dimethylbenzonitrile. Journal of the Chemical Society Perkin Transactions 2. 1003–1003.

Bloomfield, C., et al.. (1983). Electrophilic aromatic substitution. Part 28. The mechanism of nitration of some 4-substituted anisoles and phenols, and of rearrangement of the intermediate 4-nitro-4-substituted-cyclohexa-2,5-dienones. Journal of the Chemical Society Perkin Transactions 2. 75–75. 5 indexed citations

Moodie, Roy B., et al.. (1981). Electrophilic aromatic substitution. Part 27. Chemical selectivities disguised by mass diffusion. Part 6. The kinetics of nitration in aqueous sulphuric acid of durene (1,2,4,5-tetramethylbenzene), nitrodurene, and nitroprehnitene (nitro-1,2,3,4-tetramethylbenzene). A comparison of the rates of nitration of methylnitrobenzenes in aqueous sulphuric acid with the corresponding rates from mixing–disguised nitrations with nitronium hexafluorophosphate in nitromethane based on a theoretical mixing–reaction model. Journal of the Chemical Society Perkin Transactions 2. 1358–1366. 5 indexed citations

Main, Lyndsay, et al.. (1981). Electrophilic aromatic substitution. Part 26. The kinetics and mechanism of nitration of some reactive benzene derivatives in aqueous phosphoric acid. The identification of steps rate-limited by nitronium ion formation and by diffusion. Journal of the Chemical Society Perkin Transactions 2. 848–848. 2 indexed citations

Moodie, Roy B., et al.. (1980). Electrophilic aromatic substitution. Part 24. The nitration of isopropylbenzene, 2- and 4-isopropyltoluene, 1-chloro-4-isopropylbenzene, 4-isopropylanisole, and 2-bromotoluene: nitrodeisopropylation. Journal of the Chemical Society Perkin Transactions 2. 1606–1606. 3 indexed citations

10.

Barnett, James W., Roy B. Moodie, Kenneth Schofield, Peter G. Taylor, & John B. Weston. (1979). Electrophilic aromatic substitution. Part 22. The nitration of some reactive aromatics in methanesulphonic acid, and the question of positional selectivity in encounter rate nitrations of substituted naphthalenes and 1,2-diphenylethanes. Journal of the Chemical Society Perkin Transactions 2. 747–747. 3 indexed citations

11.

Moodie, Roy B., et al.. (1978). Mechanism of formation of 4-methyl- and 4-chloro-2-nitrophenol in the nitration of 4-methyl- and 4-chloro-anisole, respectively, in aqueous sulphuric acid. Journal of the Chemical Society Chemical Communications. 180–180. 4 indexed citations

12.

Moodie, Roy B., et al.. (1978). Electrophilic aromatic substitution. Part 20. The solvolyses in aqueous sulphuric acid of 4-methyl-4-nitrocyclohexa-2,5-dienyl acetate and some of its homologues, and their relevance to the nitration of methylbenzenes. Journal of the Chemical Society Perkin Transactions 2. 1145–1145. 1 indexed citations

13.

Moodie, Roy B., et al.. (1978). Electrophilic aromatic substitution. Part 19. The nitration of some reactive aromatic compounds in perchloric acid. Journal of the Chemical Society Perkin Transactions 2. 318–318. 5 indexed citations

14.

Moodie, Roy B., et al.. (1977). Electrophilic aromatic substitution. Part 18. Nitration of acetanilide and some analogues: a reconsideration. Journal of the Chemical Society Perkin Transactions 2. 1693–1693. 9 indexed citations

15.

Ferguson, Ian J., Kenneth Schofield, James W. Barnett, & M. R. Grimmett. (1977). Studies in azole chemistry. Part 2. Nitration of 1,4,5-trimethylimidazole 3-oxide and 1-methylpyrazole 2-oxide, and some reactions of the products. Journal of the Chemical Society Perkin Transactions 1. 672–672. 12 indexed citations

16.

Barnett, James W., et al.. (1977). Electrophilic aromatic substitution. Part 16. The nitration of anisole, o-methylanisole, and p-methylanisole in aqueous sulphuric acid. Journal of the Chemical Society Perkin Transactions 2. 248–248. 9 indexed citations

17.

Moodie, Roy B., et al.. (1977). Electrophilic aromatic substitution. Part 17. Products, kinetics, and mechanism of nitration in trifluoroacetic acid. Journal of the Chemical Society Perkin Transactions 2. 1688–1688. 2 indexed citations

18.

Ferguson, Ian J. & Kenneth Schofield. (1975). Studies in azole chemistry. Part I. Syntheses and reactions of some imidazole 3-oxides. Journal of the Chemical Society Perkin Transactions 1. 275–275. 28 indexed citations

19.

Moodie, Roy B., Kenneth Schofield, & John B. Weston. (1974). Positional selectivity in aromatic nitration occurring at the diffusion rate. Journal of the Chemical Society Chemical Communications. 382–382. 2 indexed citations

20.

Schofield, Kenneth, et al.. (1967). Heteroaromatic Nitrogen Compounds: The Azoles. Medical Entomology and Zoology. 65 indexed citations

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