| Year |
Citation |
Score |
| 1998 |
Yang S, Stock LM. Hydrogenation of aromatic compounds with a rhodium catalyst in biphasic systems Energy and Fuels. 12: 644-648. DOI: 10.1021/Ef9702198 |
0.361 |
|
| 1997 |
Stock LM, Obeng M. Oxidation and decarboxylation. A reaction sequence for the study of aromatic structural elements in pocahontas no. 3 coal Energy and Fuels. 11: 987-997. DOI: 10.1021/Ef960229T |
0.348 |
|
| 1993 |
Stock LM, Chatterjee K. Organic desulfurization of Illinois No. 6 coal Coal Science and Technology. 21: 291-296. DOI: 10.1016/B978-0-444-81476-0.50029-6 |
0.342 |
|
| 1991 |
Cheng C, Stock LM. Photochemical anion-promoted carbon-sulfur cleavage reactions of diaryl sulfides, alkyl aryl sulfides, and related sulfoxides and sulfones Journal of Organic Chemistry. 56: 2436-2443. DOI: 10.1021/Jo00007A034 |
0.396 |
|
| 1991 |
Stock LM, Cheng C. Preparation of deuterium-labeled petroleum residuum and asphaltene Energy & Fuels. 5: 934-936. DOI: 10.1021/Ef00030A025 |
0.346 |
|
| 1991 |
Ceylan K, Stock LM. Reaction pathways during coprocessing. Reaction of Illinois no. 6 and Wyodak coals with Lloydminster and Hondo residua under mild conditions Energy & Fuels. 5: 482-487. DOI: 10.1021/Ef00027A021 |
0.344 |
|
| 1990 |
Chatterjee K, Wolny R, Stock LM. Coal desulfurization by single electron transfer reactions Energy and Fuels. 4: 402-406. DOI: 10.1021/Ef00022A012 |
0.322 |
|
| 1990 |
Chatterjee K, Miyake M, Stock LM. Coal solubilization. Promotion of the C-alkylation reaction by n-butyllithium and potassium tert-butoxide Energy and Fuels. 4: 242-248. DOI: 10.1021/Ef00021A005 |
0.362 |
|
| 1990 |
Ceylan K, Stock LM. Reaction pathways during coprocessing. The reactivity patterns of coals and resids in hydrogen atom transfer, carbon-carbon scission, and hydrodemethylation Fuel. 69: 1386-1393. DOI: 10.1016/0016-2361(90)90120-F |
0.352 |
|
| 1989 |
Chatterjee K, Stock LM, Zabransky RF. The pathways for thermal decomposition of aryl alkyl ethers during coal pyrolysis Fuel. 68: 1349-1353. DOI: 10.1016/0016-2361(89)90255-X |
0.346 |
|
| 1989 |
Ofosu-Asante K, Stock LM, Zabransky RF. Pathways for the decomposition of linear paraffinic materials during coal pyrolysis Fuel. 68: 567-572. DOI: 10.1016/0016-2361(89)90151-8 |
0.347 |
|
| 1986 |
Stock LM, Duran JE, Noel MG, Srinivas VR. The influence of sulfur-containing compounds on the donor solvent dissolution of Illinois coals Fuel Processing Technology. 12: 287-298. DOI: 10.1016/0378-3820(86)90082-2 |
0.383 |
|
| 1986 |
Stock LM, Wang SH. Ruthenium tetroxide catalysed oxidation of coals. The formation of aliphatic and benzene carboxylic acids Fuel. 65: 1552-1562. DOI: 10.1016/0016-2361(86)90332-7 |
0.338 |
|
| 1985 |
Stock LM, Wang SH. Ruthenium tetroxide catalysed oxidation of Illinois No. 6 coal. The formation of volatile monocarboxylic acids Fuel. 64: 1713-1717. DOI: 10.1016/0016-2361(85)90398-9 |
0.315 |
|
| 1985 |
Stock LM, Duran JE, Huang CB, Srinivas VR, Willis RS. Aspects of donor solvent coal dissolution reactions. Effects of organosulphur compounds on hydrogen transfer, decomposition of 1,3-diphenylpropane and liquefaction of Illinois coals Fuel. 64: 754-760. DOI: 10.1016/0016-2361(85)90005-5 |
0.389 |
|
| 1984 |
Rose GR, Zabransky RF, Stock LM, Huang Cb, Srinivas VR, Tse Kt. The preparation and pyrolysis of O- and C-benzylated Illinois No. 6 coal Fuel. 63: 1339-1346. DOI: 10.1016/0016-2361(84)90334-X |
0.363 |
|
| 1984 |
Alemany LB, Grant DM, Pugmire RJ, Stock LM. Solid state magnetic resonance spectra of Illinois No. 6 coal and some reductive alkylation products Fuel. 63: 513-521. DOI: 10.1016/0016-2361(84)90289-8 |
0.321 |
|
| 1984 |
Hsiang-Hui K, Stock LM. Aspects of the chemistry of donor solvent coal dissolution. Promotion of the bond cleavage reactions of diphenylalkanes and the related ethers and amines Fuel. 63: 810-815. DOI: 10.1016/0016-2361(84)90072-3 |
0.433 |
|
| 1984 |
Choi CY, Stock LM. Aspects of the chemistry of donor solvent coal dissolution reactions. The reduction of benzophenone and the disproportionation of benzhydrol in hydrocarbon solvents at high temperature Journal of Organic Chemistry. 49: 2871-2875. DOI: 10.1002/Chin.198502123 |
0.344 |
|
| 1982 |
Stock LM, Hung M. The Reactions of Benzenediazonium Ions with Some Purines and Pyrimidines. Cheminform. 13: 67. DOI: 10.3987/S(B)-1982-01-0067 |
0.301 |
|
| 1982 |
Hung MH, Stock LM. Reactions of benzenediazonium ions with guanine and its derivatives Journal of Organic Chemistry. 47: 448-453. DOI: 10.1021/Jo00342A014 |
0.319 |
|
| 1982 |
Handy CI, Stock LM. Reductive alkylation of Illinois No. 6 coal in liquid ammonia Fuel. 61: 700-706. DOI: 10.1016/0016-2361(82)90242-3 |
0.399 |
|
| 1982 |
King HH, Stock LM. Aspects of the chemistry of donor solvent coal dissolution. The role of phenol in the reaction Fuel. 61: 1172-1174. DOI: 10.1016/0016-2361(82)90210-1 |
0.418 |
|
| 1982 |
Hung MH, Stock LM. Thermal decomposition of 1,4-diphenylbutane Fuel. 61: 1161-1163. DOI: 10.1016/0016-2361(82)90205-8 |
0.301 |
|
| 1982 |
Alemany LB, Stock LM. Reductive alkylation of illinois No. 6 coal. 1H and 13C n.m.r. spectra of the 13C-enriched alkylation products Fuel. 61: 1088-1094. DOI: 10.1016/0016-2361(82)90191-0 |
0.332 |
|
| 1982 |
King HH, Stock LM. Aspects of the chemistry of donor solvent coal dissolution. The hydrogen-deuterium exchange reactions of tetralin-d12 with Illinois No. 6 coal, coal products and related compounds Fuel. 61: 257-264. DOI: 10.1016/0016-2361(82)90122-3 |
0.36 |
|
| 1982 |
Alemany LB, Stock LM. The reductive alkylation of Illinois No. 6 coal. Factors governing the reductive alkylation reaction in ethereal solvents Fuel. 61: 250-256. DOI: 10.1016/0016-2361(82)90121-1 |
0.397 |
|
| 1981 |
Chin A, Hung MH, Stock LM. Reactions of benzenediazonium ions with adenine and its derivatives Journal of Organic Chemistry. 46: 2203-2207. DOI: 10.1021/Jo00324A001 |
0.318 |
|
| 1981 |
Stock LM, Tse KT, Vorvick LJ, Walstrum SA. Palladium(II) acetate catalyzed aromatic substitution reaction Journal of Organic Chemistry. 46: 1757-1759. DOI: 10.1021/Jo00321A055 |
0.402 |
|
| 1981 |
Hsiang-Hui K, Stock LM. Hydrogen transfer reactions of 1,2- and 1,4-dihydronaphthalene Fuel. 60: 748-749. DOI: 10.1016/0016-2361(81)90232-5 |
0.311 |
|
| 1980 |
Stock LM, Wright TL. Selectivity of the aromatic plumbylation reaction Journal of Organic Chemistry. 45: 4645-4648. DOI: 10.1021/Jo01311A019 |
0.732 |
|
| 1980 |
Snyder JK, Stock LM. Influences of alkyl groups on the rates of decomposition of N-nitrosoureas in basic aqueous solution Journal of Organic Chemistry. 45: 4494-4496. DOI: 10.1021/Jo01310A044 |
0.526 |
|
| 1980 |
Snyder JK, Stock LM. Reactions of alkylnitrosoureas in aqueous solution Journal of Organic Chemistry. 45: 1990-1999. DOI: 10.1021/Jo01298A048 |
0.581 |
|
| 1980 |
Snyder JK, Stock LM. Conformational preferences in alkylnitrosoureas Journal of Organic Chemistry. 45: 886-891. DOI: 10.1021/Jo01293A023 |
0.483 |
|
| 1980 |
King HH, Stock LM. Influence of Illinois No. 6 coal and coal-related compounds on the exchange reaction between diphenylmethane and perdeuteriotetralin Fuel. 59: 447-449. DOI: 10.1016/0016-2361(80)90204-5 |
0.334 |
|
| 1979 |
Stock LM, Wright TL. Mercury salt catalyzed nitration of benzene derivatives Journal of Organic Chemistry. 44: 3467-3470. DOI: 10.1021/Jo01334A004 |
0.734 |
|
| 1979 |
Kwok PY, Stock LM, Wright TL. Partial rate factors for the thallation of toluene Journal of Organic Chemistry. 44: 2309-2311. DOI: 10.1021/Jo01327A068 |
0.7 |
|
| 1978 |
Luh TY, Stock LM. Thermolysis of tert-butyl cubanepercarboxylate. The cubyl radical Journal of Organic Chemistry. 43: 3271-3273. DOI: 10.1021/Jo00411A004 |
0.625 |
|
| 1978 |
Alemany LB, King SR, Stock LM. Proton and carbon n.m.r. spectra of butylated coal Fuel. 57: 738-748. DOI: 10.1016/0016-2361(78)90132-1 |
0.365 |
|
| 1977 |
Stock LM, Wright TL. Mercuric salt catalyzed nitration of toluene Journal of Organic Chemistry. 42: 2875-2879. DOI: 10.1021/Jo00437A020 |
0.731 |
|
| 1977 |
Luh TY, Stock LM. Photoreduction of bridgehead halides with organotin hydride Journal of Organic Chemistry. 42: 2790-2792. DOI: 10.1021/Jo00436A036 |
0.664 |
|
| 1977 |
Stock LM, Wasielewski MR. Contact chemical shifts for the carbon atoms of nickel complexes of the 4-alkylanilines. The factors governing the EPR hyperfine constants of carbon atoms Journal of the American Chemical Society. 99: 50-59. DOI: 10.1002/Chin.197714042 |
0.421 |
|
| 1976 |
Stock LM, Wasielewski MR. Preparation of 9,10-difluoroanthracene The Journal of Organic Chemistry. 41: 1660-1661. DOI: 10.1002/Chin.197636196 |
0.426 |
|
| 1975 |
Stock LM, Wasielewski MR. Electron paramagnetic resonance spectra of .alpha.-substituted nitrotoluene anion radicals. Influence of electron-withdrawing substituents on the coupling constants for .beta.-hydrogen atoms Journal of the American Chemical Society. 97: 5620-5622. DOI: 10.1021/Ja00852A071 |
0.44 |
|
| 1975 |
Stock L, Wasielewski M. Additions and Corrections - Angular Dependence of β-Carbon Atom Hyperfine Coupling Constants. Journal of the American Chemical Society. 97: 1988-1988. DOI: 10.1021/Ja00840A609 |
0.414 |
|
| 1975 |
STOCK LM, WASIELEWSKI MR. ChemInform Abstract: THE ELECTRON PARAMAGNETIC RESONANCE SPECTRA OF ALPHA-SUBSTITUTED NITROTOLUENE ANION RADICALS. THE INFLUENCE OF ELECTRON-WITHDRAWING SUBSTITUENTS ON THE COUPLING CONSTANTS FOR BETA-HYDROGEN ATOMS Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197549065 |
0.444 |
|
| 1974 |
Luh T, Stock LM. Kinetic acidity of cubane Journal of the American Chemical Society. 96: 3712-3713. DOI: 10.1021/Ja00818A090 |
0.631 |
|
| 1974 |
Stock LM, Wasielewski MR. Angular dependence of .beta.-carbon atom hyperfine coupling constants Journal of the American Chemical Society. 96: 583-585. DOI: 10.1002/Chin.197414075 |
0.41 |
|
| 1973 |
Stock LM, Wasielewski MR. Pseudocontact and contact shifts for 6-aminobenzobicyclo[2.2.2]octene and 2-aminotriptycene. Sign of Bo Journal of the American Chemical Society. 95: 2743-2744. DOI: 10.1021/Ja00789A087 |
0.378 |
|
| 1973 |
STOCK LM, WASIELEWSKI MR. ChemInform Abstract: PSEUDOKONTAKT- UND KONTAKT-VERSCHIEBUNGEN FUER 6-AMINO-BENZOBICYCLO(2,2,2)OCTEN UND 2-AMINO-TRIPTYCEN, DAS VORZEICHEN VON B(0)(1) Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197326068 |
0.411 |
|
| 1973 |
STOCK LM, WASIELEWSKI MR. ChemInform Abstract: PSEUDOKONTAKT- UND KONTAKTVERSCHIEBUNGEN FUER 4-AMINO-PHENYLCYCLOPROPANDERIVATE, VORZEICHEN FUER DIE LONG RANGE-EPR-KOPPLUNGSKONSTANTEN Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197304067 |
0.416 |
|
| 1972 |
Stock LM, Luh T. Preparation of 1,4-dicarboxycubane The Journal of Organic Chemistry. 37: 338-339. DOI: 10.1021/Jo00967A044 |
0.622 |
|
| 1972 |
Stock LM, Wasielewski MR. Pseudocontact and contact shifts for 4-aminophenylcyclopropane derivatives. Signs for the long-range electron paramagnetic resonance coupling constants Journal of the American Chemical Society. 94: 8276-8277. DOI: 10.1021/Ja00778A081 |
0.423 |
|
| 1972 |
Anderson GL, Parish RC, Stock LM. Uebertragung Von Substituenteneffekten In Anthracen, Dissoziationskonstanten Von 9-Anthroesaeuren Und Chemische Verschiebungen Der Substituenten Von 9-Fluor-Anthracenen Cheminform. 3. DOI: 10.1002/Chin.197208075 |
0.507 |
|
| 1971 |
Stock LM, Wasielewski MR. Bromination of tert-butylbenzene in trifluoroacetic acid. Meta partial rate factor The Journal of Organic Chemistry. 36: 1002-1003. DOI: 10.1021/Jo00806A035 |
0.465 |
|
| 1971 |
Anderson GL, Parish RC, Stock LM. Transmission of substituent effects in anthracene. Acid dissociation constants of 10-substituted-9-anthroic acids and substituent chemical shifts of 10-substituted-9-fluoroanthracenes. Evidence for the π inductive effect Journal of the American Chemical Society. 93: 6984-6988. DOI: 10.1021/Ja00754A049 |
0.581 |
|
| 1970 |
Stock L, Wasielewski M. On the Stereochemistry of JHF The Journal of Organic Chemistry. 35: 4240-4241. DOI: 10.1021/Jo00837A627 |
0.453 |
|
| 1970 |
Anderson GL, Stock LM. Chemie Der Bicyclo(2,2,2)Octane 9. Mitt. Chemische Verschiebungen Von Bicyclischen Fluoriden Cheminform. 1. DOI: 10.1002/Chin.197009014 |
0.529 |
|
| 1969 |
Himoe A, Stock LM. Rates and relative rates of chlorination of benzene, toluene, and t-butylbenzene in carboxylic acid solvents. The influence of solvent on the Baker-Nathan effect Journal of the American Chemical Society. 91: 1452-1457. DOI: 10.1021/Ja01034A031 |
0.331 |
|
| 1968 |
Anderson GL, Stock LM. Chemistry of the bicyclo[2.2.2]octanes. IX. Chemical shifts for bicyclic fluorides Journal of the American Chemical Society. 90: 6804-6808. DOI: 10.1021/Ja01052A044 |
0.54 |
|
| 1967 |
Baker FW, Stock LM. Preparation of 4-substituted bicyclo[2.2.2]oct-2-ene-1-carboxylic acids Journal of Organic Chemistry. 32: 3344-3348. DOI: 10.1021/Jo01286A015 |
0.34 |
|
| 1965 |
Holtz HD, Stock LM. Rates of reaction of 4-substituted bicyclo [2.2.2]octylmethyl tosylates with sodium thiophenolate. The role of polar effects in the displacement reaction Journal of the American Chemical Society. 87: 2404-2409. DOI: 10.1021/Ja01089A019 |
0.38 |
|
| 1964 |
Holtz HD, Stock LM. Dissociation constants for 4-substituted bicyclo[2.2.2]octane-1-carboxylic acids. Empirical and theoretical analysis Journal of the American Chemical Society. 86: 5188-5194. DOI: 10.1021/Ja01077A031 |
0.331 |
|
| 1964 |
Holtz HD, Stock LM. The preparation of 1-carboxy-4-substituted bicyclo[2.2.2]octanes Journal of the American Chemical Society. 86: 5183-5188. DOI: 10.1021/Ja01077A030 |
0.345 |
|
| 1963 |
Baker FW, Holtz HD, Stock LM. The brominative decarboxylation of bicyclo[2.2.2]octane-1-carboxylic acid in halogenated solvents Journal of Organic Chemistry. 28: 514-516. DOI: 10.1021/Jo01037A062 |
0.332 |
|
| 1963 |
Stock LM, Brown HC. A Quantitative Treatment of Directive Effects in Aromatic Substitution Advances in Physical Organic Chemistry. 1: 35-154. DOI: 10.1016/S0065-3160(08)60277-4 |
0.471 |
|
| 1962 |
Brown HC, Stock LM. A Critical Examination of the Applicability of A Linear Free Energy Relationship to Aromatic Substitution Reactions Journal of the American Chemical Society. 84: 3298-3306. DOI: 10.1021/Ja00876A017 |
0.426 |
|
| 1962 |
Stock LM, Baker FW. Rates and isomer distributions in the non-catalytic chlorination of the halobenzenes and certain halotoluenes in aqueous acetic acid. Partial rate factors for the halogenation of the halobenzenes Journal of the American Chemical Society. 84: 1661-1667. DOI: 10.1021/Ja00868A034 |
0.336 |
|
| 1962 |
Stock LM, Brown HC. An Examination of the Applicability of the Selectivity Relationship to the Electrophilic Substitution Reactions of Biphenyl and Fluorene1-3 Journal of the American Chemical Society. 84: 1242-1248. DOI: 10.1021/Ja00866A036 |
0.463 |
|
| 1962 |
Brown HC, Stock LM. Relative Rates and Isomer Distributions in the Bromination of Biphenyl and Fluorene in Acetic Acid. Partial Rate Factors for the Bromination Reaction1-3 Journal of the American Chemical Society. 84: 1238-1241. DOI: 10.1021/Ja00866A035 |
0.479 |
|
| 1961 |
Stock LM, Himoe A. Rates, Relative Rates and Product Distributions for the Non-catalytic Chlorination of Benzene, Toluene and t-Butylbenzene in Certain Non-aqueous Non-hydroxylic Solvents. The Influence of Solvent on the Reaction and the Baker-Nathan Effect Journal of the American Chemical Society. 83: 4605-4609. DOI: 10.1021/Ja01483A024 |
0.351 |
|
| 1961 |
Stock LM, Himoe A. Rates and Isomer Distributions in the Chlorination of Benzene, Toluene and t-Butylbenzene in Aqueous Acetic Acid Solvents. The Influence of Solvent on the Reaction and the Baker-Nathan Effect Journal of the American Chemical Society. 83: 1937-1944. DOI: 10.1021/Ja01469A038 |
0.381 |
|
| 1960 |
Stock LM, Brown HC. Rates of Bromination of Anisole and Certain Derivatives. Partial Rate Factors for the Bromination Reaction. The Application of the Selectivity Relationship to the Substitution Reactions of Anisole1,2 Journal of the American Chemical Society. 82: 1942-1947. DOI: 10.1021/Ja01493A026 |
0.494 |
|
| 1959 |
Stock L, Brown H. Additions and Corrections: The Selectivity Relationship. An Examination of the Electrophilic Substitution, Electrophilic Side-Chain and Hammett Side-Chain Reactions of Toluene and Tolyl Derivatives. Journal of the American Chemical Society. 81: 6537-6537. DOI: 10.1021/Ja01533A649 |
0.447 |
|
| 1959 |
Stock LM, Brown HC. Relative Rates and Isomer Distributions in the Halogenation of t-Butylbenzene and Some of Its Derivatives. Partial Rate Factors for Non-catalytic Bromination and Chlorination in Acetic Acid1-3 Journal of the American Chemical Society. 81: 5615-5620. DOI: 10.1021/Ja01530A024 |
0.44 |
|
| 1959 |
Stock LM, Brown HC. The Selectivity Relationship. An Examination of the Electrophilic Substitution, Electrophilic Side-chain and Hammett Side-chain Reactions of Toluene and Tolyl Derivatives1-3 Journal of the American Chemical Society. 81: 3323-3329. DOI: 10.1021/Ja01522A043 |
0.431 |
|
| 1959 |
Brown HC, Marino G, Stock LM. The Relative Rate and Isomer Distribution in the Acetylation of Benzene and Toluene in Ethylene Dichloride under the Influence of Aluminum Chloride1,2 Journal of the American Chemical Society. 81: 3310-3314. DOI: 10.1021/Ja01522A040 |
0.403 |
|
| 1959 |
Stock LM, Brown HC. An Examination of the Applicability of the Selectivity Relationship to the Electrophilic Substitution Reactions of the Halobenzenes Journal of the American Chemical Society. 81: 1668-1673. DOI: 10.1021/Ja00868A035 |
0.461 |
|
| 1957 |
Brown HC, Stock LM. Rates of Chlorination of Benzene, Toluene and the Xylenes. Partial Rate Factors for the Chlorination Reaction1,2,3 Journal of the American Chemical Society. 79: 5175-5179. DOI: 10.1021/Ja01576A025 |
0.467 |
|
| 1957 |
Brown HC, Stock LM. Relative Rates of Bromination of Benzene and the Methylbenzenes. Partial Rate Factors for the Bromination Reaction1-3 Journal of the American Chemical Society. 79: 1421-1425. DOI: 10.1021/Ja01563A040 |
0.464 |
|
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