| Year |
Citation |
Score |
| 2015 |
Saunders WH, Gronert S. The Competition between Elimination Pathways in the Reactions of a Wide Variety of Bases with 2-Fluoro- and 2-Chlorobutane in the Gas Phase. The Journal of Organic Chemistry. 80: 10787-93. PMID 26484560 DOI: 10.1021/Acs.Joc.5B01983 |
0.399 |
|
| 2010 |
Wu W, Shaik S, Saunders WH. VBSCF calculations on the bimolecular (E2) elimination reaction. The nature of the transition state. The Journal of Organic Chemistry. 75: 3722-8. PMID 20465312 DOI: 10.1021/Jo100465J |
0.348 |
|
| 2000 |
Harris N, Wei W, Saunders WH, Shaik S. Origins of nonperfect synchronization in the lowest-energy path of identity proton transfer reactions leading to delocalized anions a vbscf study Journal of the American Chemical Society. 122: 6754-6758. DOI: 10.1021/Ja001032P |
0.366 |
|
| 1999 |
Saunders WH. Negative Ion Hyperconjugation in Fluorocarbanions and the Nature of the Borderline between E1cB and E2 Mechanisms. An ab Initio Study. The Journal of Organic Chemistry. 64: 861-865. PMID 11674158 DOI: 10.1021/Jo981769L |
0.302 |
|
| 1999 |
Harris N, Wei W, Saunders WH, Shaik S. Origins of non-perfect synchronization in the lowest energy path of the identity proton transfer reaction of allyl anion + propene: A VBSCF study Journal of Physical Organic Chemistry. 12: 259-262. DOI: 10.1002/(Sici)1099-1395(199903)12:3<259::Aid-Poc153>3.0.Co;2-H |
0.394 |
|
| 1998 |
Van Verth JE, Saunders WH. Proton Transfers from ZCH(3) to ZCH(2)(-) (Z = F, Cl, Br, OH, SH, SeH). An ab Initio Investigation. The Journal of Organic Chemistry. 63: 209. PMID 11674068 DOI: 10.1021/Jo974028D |
0.327 |
|
| 1998 |
Van Verth JE, Saunders WH, Kermis TW. Identity-reaction proton transfers from nitrogen acids yielding localized vs. delocalized conjugate bases. An ab initio study Canadian Journal of Chemistry. 76: 821-827. DOI: 10.1139/V98-053 |
0.303 |
|
| 1997 |
Saunders WH. Negative Ion Hyperconjugation and Its Relevance to the Mechanism of E1cB Reactions. An ab Initio Study. The Journal of Organic Chemistry. 62: 244-245. PMID 11671395 DOI: 10.1021/Jo9611778 |
0.408 |
|
| 1995 |
Saunders WH, Van Verth JE. Ab initio comparison of identity-reaction proton transfers from carbon acids yielding localized vs delocalized conjugate bases Journal of Organic Chemistry. 60: 3452-3458. DOI: 10.1021/Jo00116A036 |
0.397 |
|
| 1994 |
Lin S, Saunders W. Correction. Tunneling in Elimination Reactions. Structural Effects on the Secondary β-Tritium Isotope Effect Journal of the American Chemical Society. 116: 9809-9809. DOI: 10.1021/Ja00100A600 |
0.393 |
|
| 1994 |
Kupczyk-Subotkowska L, Saunders WH, Shine HJ, Subotkowski W. Carbon kinetic isotope effects and transition structures in the rearrangements of allyl vinyl ethers. 2-(trimethylsiloxy)- and 2-(methoxycarbonyl)-3-oxa-1,5-hexadiene Journal of the American Chemical Society. 116: 7088-7093. DOI: 10.1021/Ja00095A011 |
0.349 |
|
| 1994 |
Lin S, Saunders WH. Tunneling In Elimination Reactions. Structural Effects On The Secondary Beta -Tritium Isotope Effect Journal of the American Chemical Society. 116: 6107-6110. DOI: 10.1021/Ja00093A007 |
0.369 |
|
| 1993 |
Kupczyk-Subotkowska L, Saunders WH, Shine HJ, Subotkowski W. Thermal rearrangement of allyl vinyl ether: Heavy-atom kinetic isotope effects and the transition structure Journal of the American Chemical Society. 115: 5957-5961. DOI: 10.1021/Ja00067A009 |
0.322 |
|
| 1992 |
Ašperger S, Kukri? Z, Saunders WH, Šuti? D. High secondary α-deuterium kinetic isotope effect in the acetolysis and formolysis of dideuterioferrocenylmethyl benzoate Journal of the Chemical Society, Perkin Transactions 2. 275-279. DOI: 10.1039/P29920000275 |
0.303 |
|
| 1992 |
Kupczyk-Subotkowska L, Subotkowski W, Saunders WH, Shine HJ. Claisen rearrangement of allyl phenyl ether. 1-carbon-14 and .beta.-carbon-14 kinetic isotope effects. A clearer view of the transition structure Journal of the American Chemical Society. 114: 3441-3445. DOI: 10.1021/Ja00035A042 |
0.315 |
|
| 1991 |
Xie L, Saunders WH. Unusual induced isotope effects in the reaction of 2-pentanone with dialkylamide bases. Evidence on the nature of the reactive base species Journal of the American Chemical Society. 113: 3123-3130. DOI: 10.1021/Ja00008A047 |
0.37 |
|
| 1990 |
Amin M, Price RC, Saunders WH. Tunneling in elimination reactions. Tests of criteria for tunneling predicted by model calculations Journal of the American Chemical Society. 112: 4467-4471. DOI: 10.1021/Ja00167A052 |
0.333 |
|
| 1989 |
Beutelman HP, Xie L, Saunders WH. Deuterium isotope effects and the mechanism of kinetic enolate formation Journal of Organic Chemistry. 54: 1703-1709. DOI: 10.1021/Jo00146A049 |
0.478 |
|
| 1988 |
Amin M, Price RC, Saunders WH. Isotope effects on isotope effects. Failure of the rule of the geometric mean as evidence for tunneling Journal of the American Chemical Society. 110: 4085-4086. DOI: 10.1021/Ja00220A084 |
0.354 |
|
| 1986 |
Green MM, Boyle BA, Vairamani M, Mukhopadhyay T, Saunders WH, Bowen P, Allinger NL. Temperature-dependent stereoselectivity and hydrogen deuterium kinetic isotope effect for .gamma.-hydrogen transfer to 2-hexyloxy radical. The transition state for the Barton reaction. Journal of the American Chemical Society. 108: 2381-7. PMID 22175587 DOI: 10.1021/Ja00269A040 |
0.345 |
|
| 1986 |
Dohner BR, Saunders WH. Mechanisms of elimination reactions. 40. Attempted study of stereochemistry of elimination from 2-(p-nitropheny1)ethyltrimethylammonium ion. Base-promoted cis-trans isomerization of p-nitrostyrene-β-d1 Canadian Journal of Chemistry. 64: 1026-1030. DOI: 10.1139/V86-172 |
0.347 |
|
| 1986 |
Saunders WH. Correction. Contribution of Tunneling to Secondary Isotope Effects in Proton-Transfer Reactions. Journal of the American Chemical Society. 108: 5041-5041. DOI: 10.1021/Ja00276A600 |
0.442 |
|
| 1986 |
Dohner BR, Saunders WH. Mechanisms of elimination reactions. XXXIX: Steric and electronic effects on stereochemistry in eliminations from primary alkyltrimethylammonium salts Journal of the American Chemical Society. 108: 245-247. DOI: 10.1021/Ja00262A010 |
0.33 |
|
| 1986 |
Dohner BR, Saunders WH. Mechanisms of elimination reactions. 39. Steric and electronic effects on stereochemistry in eliminations from primary alkyltrimethylammonium salts Journal of the American Chemical Society. 108: 245-247. |
0.305 |
|
| 1985 |
Wu SL, Hargreaves RT, Saunders WH. .alpha.-14C and sulfur-34 isotope effects in E2 reactions of (2-phenylethyl)dimethylsulfonium ion Journal of Organic Chemistry. 50: 2392-2394. DOI: 10.1021/Jo00213A043 |
0.307 |
|
| 1985 |
Zhou P, Vitale AA, San Filippo J, Saunders WH. Kinetic isotope effect associated with the dissociative addition of dihydrogen to trans-Ir(CO)Cl(Ph3P)2 Journal of the American Chemical Society. 107: 8049-8054. DOI: 10.1021/Ja00312A042 |
0.326 |
|
| 1985 |
Saunders WH. Calculations of isotope effects in elimination reactions. New experimental criteria for tunneling in slow proton transfers Journal of the American Chemical Society. 107: 164-169. DOI: 10.1021/Ja00287A029 |
0.341 |
|
| 1984 |
Wu SL, Tao YT, Saunders WH. Mechanisms of elimination reactions. 38. Why is the effect of successive β-alkyl substitution on the rates of elimination from quaternary ammonium salts nonadditive? Journal of the American Chemical Society. 106: 7583-7588. DOI: 10.1021/Ja00336A045 |
0.37 |
|
| 1984 |
Subramanian R, Saunders WH. Mechanisms of elimination reactions. 37. Secondary β-tritium isotope effects in eliminations from 2-arylethyl derivatives Journal of the American Chemical Society. 106: 7887-7890. |
0.314 |
|
| 1984 |
Saunders WH. Contribution of tunneling to secondary isotope effects in proton-transfer reactions Journal of the American Chemical Society. 106: 2223-2224. |
0.344 |
|
| 1983 |
Engdahl KA, Bivehed H, Ahlberg P, Saunders WH. Rate-controlling two-proton transfer coupled with heavy-atom motion in the 2-pyridinone-catalyzed mutarotation of tetramethylglucose. Experimental and calculated deuterium isotope effects Journal of the American Chemical Society. 105: 4767-4774. DOI: 10.1021/Ja00352A040 |
0.311 |
|
| 1983 |
Tao YT, Saunders WH. Mechanisms of elimination reactions. 36. Stereochemistry and transition-state structure in eliminations from primary alkyltrimethylammonium salts Journal of the American Chemical Society. 105: 3183-3188. DOI: 10.1021/Ja00348A037 |
0.401 |
|
| 1982 |
Engdahl KA, Bivehed H, Ahlberg P, Saunders WH. Simultaneous proton transfers coupled with heavy atom motion in the transition state of the 2-pyridone-catalysed mutarotation of tetramethylglucose. Primary and secondary deuterium isotope effects Journal of the Chemical Society, Chemical Communications. 423-425. DOI: 10.1039/C39820000423 |
0.305 |
|
| 1981 |
Miller DJ, Saunders WH. Mechanisms of elimination reactions. 35. Deuterium kinetic isotope effects and tunneling in the reaction of [2-[p-(trifluoromethyl)phenyl]ethyl]trimethylammonium ion with hydroxide ion in mixtures of water and dimethyl sulfoxide Journal of Organic Chemistry. 46: 4247-4252. DOI: 10.1021/Jo00334A028 |
0.351 |
|
| 1981 |
Brown KC, Romano FJ, Saunders WH. Mechanisms of elimination reactions. 34. Deuterium and nitrogen isotope effects and Hammett correlations in the reaction of (2-arylethyl)trimethylammonium ions with hydroxide ion in mixtures of water and dimethyl sulfoxide Journal of Organic Chemistry. 46: 4242-4246. DOI: 10.1021/Jo00334A027 |
0.349 |
|
| 1981 |
Miller DJ, Subramanian R, Saunders WH. Mechanisms of elimination reactions. 33. Carbon isotope effects in E2 reactions of (2-phenylethyl-2-14C)trimethylammonium ion. The role of tunneling Journal of the American Chemical Society. 103: 3519-3522. DOI: 10.1021/Ja00402A043 |
0.378 |
|
| 1981 |
Subramanian R, Saunders WH. How to measure both primary and secondary hydrogen isotope effects in hydrogen abstraction from a substrate having two or more equivalent reactive hydrogen atoms Journal of Physical Chemistry. 85: 1099-1100. DOI: 10.1021/J150609A005 |
0.386 |
|
| 1980 |
Chiao WB, Saunders WH. Mechanisms of elimination reactions. 31. Stereochemistry of elimination reactions of 3-phenyl-2-butyl tosylates Journal of Organic Chemistry. 45: 1319-1320. DOI: 10.1021/Jo01295A034 |
0.471 |
|
| 1980 |
Kaldor SB, Fredenburg ME, Saunders WH. Mechanisms of elimination reactions. 32. Tritium isotope effects and tunnel effects in the reaction of 2,2-diphenylethyl-2-t derivatives with various bases Journal of the American Chemical Society. 102: 6296-6299. DOI: 10.1021/Ja00540A020 |
0.462 |
|
| 1980 |
Wilson JC, Källsson I, Saunders WH. Carbon isotope effects in proton abstraction from 2-nitropropane-2-14C by pyridines. The contribution of tunneling Journal of the American Chemical Society. 102: 4780-4784. DOI: 10.1021/Ja00534A034 |
0.375 |
|
| 1979 |
Kaldor SB, Saunders WH. Mechanisms of elimination reactions. 30. The contributions of tunneling and heavy-atom motion in the reaction coordinate to deuterium kinetic isotope effects in eliminations from 2-phenylethyl derivatives Journal of the American Chemical Society. 101: 7594-7599. DOI: 10.1021/Ja00519A021 |
0.364 |
|
| 1979 |
Miller DJ, Saunders WH. Contribution of tunneling to relative reactivity in an elimination reaction Journal of the American Chemical Society. 101: 6749-6750. DOI: 10.1021/Ja00516A046 |
0.449 |
|
| 1979 |
Miller DJ, Saunders WH. Contribution of tunneling to relative reactivity in an elimination reaction [6] Journal of the American Chemical Society. 101: 6749-6750. |
0.348 |
|
| 1978 |
Chiao WB, Saunders WH. Mechanisms of elimination reactions. 29. Deuterium kinetic isotope effects in eliminations from amine oxides. The consequences of nonlinear proton transfer Journal of the American Chemical Society. 100: 2802-2805. DOI: 10.1021/Ja00477A037 |
0.409 |
|
| 1977 |
Chiao WB, Saunders WH. Mechanism of elimination reactions. 28. Stereochemistry of elimination reactions of 2- and 3-hexyl tosylates Journal of the American Chemical Society. 99: 6699-6703. DOI: 10.1021/Ja00462A037 |
0.464 |
|
| 1977 |
Roe FL, Saunders WH. Mechanisms of elimination reactions-XXVII. The reactions of 1-arylethyldimethylsulfonium bromides with sodium ethoxide in ethanol Tetrahedron. 33: 1581-1585. DOI: 10.1016/0040-4020(77)80165-8 |
0.307 |
|
| 1977 |
Saunders WH, Bonadies SD, Braunstein M, Borchardt JK, Hargreaves RT. Mechanisms of elimination reactions-XXVI. The α'-β mechanism in elimination reactions of sulforium salts Tetrahedron. 33: 1577-1580. DOI: 10.1016/0040-4020(77)80164-6 |
0.363 |
|
| 1976 |
Montgomery FC, Saunders WH. Migration aptitudes in the photolysis of some tertiary alkyl azides Journal of Organic Chemistry. 41: 2368-2372. DOI: 10.1021/Jo00876A003 |
0.309 |
|
| 1976 |
Hargreaves RT, Katz AM, Saunders WH. Sulfur isotope effects in substitution reactions of trimethylsulfonium ion. [60/sup 0/C; reactions with bromide, thiophenoxide, ethoxide, and phenoxide] Journal of the American Chemical Society. 98: 2614-2617. DOI: 10.1021/Ja00425A034 |
0.436 |
|
| 1976 |
Hargreaves RT, Katz AM, Saunders WH. Sulfur isotope effects in substitution reactions of trimethylsulfonium ion Journal of the American Chemical Society. 98: 2614-2617. |
0.336 |
|
| 1975 |
Saunders WH. Mechanisms Of Elimination Reactions Part 24, Model Calculations Of Isotope Effects In Elimination Reactions Cheminform. 6. DOI: 10.1002/Chin.197543109 |
0.467 |
|
| 1974 |
Borchardt JK, Swanson JC, Saunders WH. Mechanisms of elimination reactions. XXIII. Stereochemistry of elimination reactions of 3-hexyl tosylate and fluoride. The role of ion pairing Journal of the American Chemical Society. 96: 3918-3920. DOI: 10.1021/Ja00819A032 |
0.452 |
|
| 1973 |
Bailey DS, Saunders WH. Mechanisms of elimination reactions. XIX. Rates and product proportions in the reactions of 2-methyl-2-butyl halides with thiolate ions Journal of Organic Chemistry. 38: 3363-3366. DOI: 10.1021/Jo00959A027 |
0.447 |
|
| 1973 |
Yarchak ML, Christopher Dalton J, Saunders WH. Mechanisms of elimination reactions. XXI. Ring-size effects and the nature of the excited states in the photolysis of cycloalkyl phenylacetates Journal of the American Chemical Society. 95: 5228-5233. DOI: 10.1021/Ja00797A022 |
0.376 |
|
| 1973 |
Yarchak ML, Christopher Dalton J, Saunders WH. Mechanisms of elimination reactions. XX. Stereochemistry of photoeliminations from some cyclic phenylacetates Journal of the American Chemical Society. 95: 5224-5227. DOI: 10.1021/Ja00797A021 |
0.461 |
|
| 1972 |
Saunders WH. Concerning driving forces for β-elimination reactions Tetrahedron Letters. 13: 5129-5132. DOI: 10.1016/S0040-4039(01)85187-X |
0.337 |
|
| 1971 |
Feit IN, Schadt F, Lubinkowski J, Saunders WH. Mechanisms of elimination reactions. XVIII. The effect of base, solvent, and structure on product ratios in E2 reactions of some sulfonium salts Journal of the American Chemical Society. 93: 6606-6609. DOI: 10.1021/Ja00753A046 |
0.448 |
|
| 1970 |
Saunders WH, Bailey DS, Montgomery FC, Chodak GW. Mechanisms of elimination reactions. XVII. Relation between stereochemistry and trans:cis ratios in eliminations from open-chain quaternary ammonium salts Journal of the American Chemical Society. 92: 6911-6913. DOI: 10.1021/Ja00726A030 |
0.379 |
|
| 1970 |
Feit IN, Saunders WH. Mechanisms of elimination reactions. XV. The effect of base, solvent, and structure on product ratios in elimination reactions of some quaternary ammonium salts Journal of the American Chemical Society. 92: 5615-5619. DOI: 10.1021/Ja00722A013 |
0.458 |
|
| 1970 |
Brown KC, Saunders WH. Mechanisms of elimination reactions. XIV. Stereochemistry and isotope effects in eliminations from cyclopentyl- and 3,3-dimethylcyclopentyltrimethylammonium salts Journal of the American Chemical Society. 92: 4292-4295. DOI: 10.1021/Ja00717A026 |
0.485 |
|
| 1970 |
Feit IN, Saunders WH. Mechanisms of elimination reactions. XIII. The effect of base, solvent, and structure on product ratios in elimination reactions of some secondary tosylates Journal of the American Chemical Society. 92: 1630-1634. DOI: 10.1021/Ja00709A035 |
0.455 |
|
| 1969 |
Saunders WH, Ashe TA. Mechanisms of elimination reactions. XII. Hydrogen isotope effects and the nature of the transition state in eliminations from alicyclic quaternary ammonium salts Journal of the American Chemical Society. 91: 4473-4478. DOI: 10.1021/Ja01044A026 |
0.42 |
|
| 1969 |
Katz AM, Saunders WH. Mechanisms of elimination reactions. XI. Theoretical calculations of isotope effects in elimination reactions Journal of the American Chemical Society. 91: 4469-4472. DOI: 10.1021/Ja01044A025 |
0.473 |
|
| 1968 |
Lewis FD, Saunders WH. Sensitized Photolysis of Organic Azides. A Possible Case of Nonclassical Energy Transfer Journal of the American Chemical Society. 90: 7033-7038. DOI: 10.1021/Ja01027A026 |
0.443 |
|
| 1968 |
Lewis FD, Saunders WH. The Intermediates in Direct Photolysis of Alkyl Azides Journal of the American Chemical Society. 90: 7031-7033. DOI: 10.1021/Ja01027A025 |
0.54 |
|
| 1968 |
Lewis FD, Saunders WH. Carbon-nitrogen cleavage in the photolysis and pyrolysis of triphenylmethyl azide Journal of the American Chemical Society. 90: 3828-3830. DOI: 10.1021/Ja01016A041 |
0.459 |
|
| 1968 |
Saunders WH, Bushman DG, Cockerill AF. Mechanisms of elimination reactions. X. Substituent, isotope, and solvent effects in E2 reactions of some 2-arylethyltrimethylammonium bromides Journal of the American Chemical Society. 90: 1775-1779. DOI: 10.1021/Ja01009A017 |
0.457 |
|
| 1967 |
Cockerill AF, Saunders WH. Mechanisms of elimination reactions. IX. The effect of added dimethyl sulfoxide on rates and sulfur isotope effects in the reaction of 2-phenylethyldimethylsulfonium bromide with hydroxide ion in water Journal of the American Chemical Society. 89: 4985-4987. DOI: 10.1021/Ja00995A027 |
0.447 |
|
| 1967 |
Cockerill AF, Rottschaefer S, Saunders WH. Mechanisms of elimination reactions. VIII. The effect of added dimethyl sulfoxide on rates, isotope effects, and substituent effects in the reaction of 2-arylethyl bromides with potassium t-butoxide in t-butyl alcohol Journal of the American Chemical Society. 89: 901-905. DOI: 10.1021/Ja00980A029 |
0.394 |
|
| 1967 |
Finley KT, Saunders WH. Mechanisms of elimination reactions. VII. Rates of elimination of some deuterated cyclohexyl tosylates Journal of the American Chemical Society. 89: 898-901. DOI: 10.1021/Ja00980A028 |
0.435 |
|
| 1967 |
Lewis FD, Saunders WH. Photosensitized rearrangements of triarylmethyl azides Journal of the American Chemical Society. 89: 645-647. DOI: 10.1021/Ja00979A031 |
0.487 |
|
| 1966 |
Saunders WH, Schreiber MR. Evidence against a carbanion mechanism for elimination reactions of alkyl fluorides Chemical Communications (London). 145-146. DOI: 10.1039/C19660000145 |
0.468 |
|
| 1966 |
Owen JR, Saunders WH. The migration aptitude of substituted benzyl vs. methyl in carbonium ion reactions of the 2,2-dimethyl-3-aryl-1-propyl system. The question of alkyl participation Journal of the American Chemical Society. 88: 5809-5816. DOI: 10.1021/Ja00976A022 |
0.408 |
|
| 1966 |
Saunders WH, Cockerill AF, Ašperger S, Klasinc L, Stefanović D. The sulfur isotope effect in the E2 reaction of 2-phenylethyldimethylsulfonium bromide with hydroxide ion. A correction [5] Journal of the American Chemical Society. 88: 848. DOI: 10.1021/Ja00956A047 |
0.412 |
|
| 1966 |
Saunders WH. Kinetic Isotope Effects Cheminform. 3: 109-146. DOI: 10.1016/B978-1-4832-0005-7.50009-7 |
0.349 |
|
| 1965 |
Saunders WH, Fahrenholtz SR, Caress EA, Lowe JP, Schreiber M. Mechanisms of elimination reactions. VI. The effect of the leaving group on orientation in E2 reactions Journal of the American Chemical Society. 87: 3401-3406. DOI: 10.1021/Ja01093A020 |
0.436 |
|
| 1964 |
Heidke RL, Saunders WH. Cleavage of 2,2-dialkyl-1,3-diols Journal of Organic Chemistry. 29: 3704-3705. DOI: 10.1021/Jo01035A511 |
0.306 |
|
| 1964 |
Saunders WH, Zimmerman SE. Mechanisms of elimination reactions. V. Sulfur isotope effects in some reactions of t-butyldimethylsulfonium iodide Journal of the American Chemical Society. 86: 3789-3791. DOI: 10.1021/Ja01072A038 |
0.446 |
|
| 1963 |
Saunders WH. Mechanisms of Organic and Enzymic Reactions. Journal of the American Chemical Society. 85: 838-838. DOI: 10.1021/Ja00889A063 |
0.367 |
|
| 1962 |
Warrick P, Saunders WH. The migration aptitude of benzyl vs. methyl in carbonium ion reactions of the 2,2-dimethyl-3-phenyl-1-propyl system Journal of the American Chemical Society. 84: 4095-4100. DOI: 10.1021/Ja00880A026 |
0.396 |
|
| 1961 |
Saunders WH, Paine RH. Phenyl vs. methyl migration aptitudes in some carbonium ion reactions of neophyl derivatives Journal of the American Chemical Society. 83: 882-885. DOI: 10.1021/Ja01465A034 |
0.392 |
|
| 1960 |
Saunders WH, Carges GL. “1,3-Shifts” in Rearrangements of 3,4,4-Trimethyl-2-pentyl Derivatives1 Journal of the American Chemical Society. 82: 3582-3585. DOI: 10.1021/Ja01499A027 |
0.303 |
|
| 1960 |
Saunders WH, Edison DH. Mechanisms of elimination reactions. IV. Deuterium isotope effects in E2 reactions of some 2-phenylethyl derivatives Journal of the American Chemical Society. 82: 138-142. DOI: 10.1021/Ja01486A031 |
0.416 |
|
| 1960 |
Saunders WH, Fahrenholtz SR, Lowe JP. The effect of the leaving group on orientation in E2 elimination reactions Tetrahedron Letters. 1: 1-3. DOI: 10.1016/S0040-4039(01)84077-6 |
0.372 |
|
| 1958 |
Saunders WH, Gibbons CB, Williams RA. Mechanisms of Elimination Reactions. III. Rates of Elimination from Some Substituted 2-Phenylethyldimethylsulfonium Bromides in Aqueous Solution1 Journal of the American Chemical Society. 80: 4099-4100. DOI: 10.1021/Ja01548A070 |
0.44 |
|
| 1958 |
Saunders WH, Ašperger S, Edison DH. Rates of Solvolysis of Some Deuterated 2-Phenylethyl p-Toluenesulfonates1,2 Journal of the American Chemical Society. 80: 2421-2424. DOI: 10.1021/Ja01543A018 |
0.313 |
|
| 1957 |
Saunders WH. Tables of Chemical Kinetics, Homogeneous Reactions. Journal of the American Chemical Society. 79: 3935-3936. DOI: 10.1021/Ja01571A098 |
0.423 |
|
| 1957 |
Saunders WH, Williams RA. Mechanisms of Elimination Reactions. II. Rates of Elimination from Some Substituted 2-Phenylethyl Bromides and 2-Phenylethyldimethylsulfonium Bromides1 Journal of the American Chemical Society. 79: 3712-3716. DOI: 10.1021/Ja01571A030 |
0.41 |
|
| 1957 |
Saunders WH, sperger SA. Mechanisms of Elimination Reactions. Sulfur Isotope Effects in the Decomposition of Some Sulfonium Salts Journal of the American Chemical Society. 79: 1612-1615. DOI: 10.1021/Ja01564A024 |
0.484 |
|
| 1955 |
Saunders WH. Steric Effects on Migration Aptitudes. Reaction of Some o-Substituted Benzophenones with Peroxyacetic Acid Journal of the American Chemical Society. 77: 4679-4681. DOI: 10.1021/Ja01622A079 |
0.375 |
|
| Show low-probability matches. |