| Year |
Citation |
Score |
| 2006 |
Jencks WP, Wolfenden RV. Fritz Albert Lipmann: June 12, 1899-July 24, 1986. Biographical Memoirs. National Academy of Sciences (U.S.). 88: 246-66. PMID 18543445 |
0.544 |
|
| 2000 |
Jencks WP, Wolfenden RV. Fritz Albert Lipmann. 12 June 1899 — 24 July 1986 Biographical Memoirs of Fellows of the Royal Society. 46: 333-344. DOI: 10.1098/Rsbm.1999.0088 |
0.593 |
|
| 1997 |
Jencks WP. From chemistry to biochemistry to catalysis to movement. Annual Review of Biochemistry. 66: 1-18. PMID 9242900 DOI: 10.1146/annurev.biochem.66.1.1 |
0.364 |
|
| 1997 |
Dalby KN, Jencks WP. General acid catalysis of the reversible addition of thiolate anions to cyanamide Journal of the Chemical Society. Perkin Transactions 2. 1555-1563. DOI: 10.1039/A700205J |
0.708 |
|
| 1997 |
Dalby KN, Jencks WP. Lifetimes of imidinium ions in aqueous solution Journal of the American Chemical Society. 119: 7271-7280. DOI: 10.1021/ja970628i |
0.637 |
|
| 1996 |
Ghosh MC, Jencks WP. Phosphorylation of the sodium-potassium adenosinetriphosphatase with adenosine triphosphate and sodium ion that requires subconformations in addition to principal E1 and E2 conformations of the enzyme. Biochemistry. 35: 12587-90. PMID 8823196 DOI: 10.1021/bi961324w |
0.31 |
|
| 1996 |
Keillor JW, Jencks WP. Phosphorylation of the sodium--potassium adenosinetriphosphatase proceeds through a rate-limiting conformational change followed by rapid phosphoryl transfer. Biochemistry. 35: 2750-3. PMID 8611581 DOI: 10.1021/Bi951370G |
0.305 |
|
| 1996 |
Jencks WP. Quantitive approaches to reaction mechanisms and catalysis. Substitution at carbon Journal of Physical Organic Chemistry. 9: 337-340. DOI: 10.1002/(Sici)1099-1395(199606)9:6<337::Aid-Poc803>3.0.Co;2-P |
0.327 |
|
| 1995 |
Jencks WP. The mechanism of coupling chemical and physical reactions by the calcium ATPase of sarcoplasmic reticulum and other coupled vectorial systems. Bioscience Reports. 15: 283-7. PMID 8825030 DOI: 10.1007/BF01788360 |
0.313 |
|
| 1995 |
Myung J, Jencks WP. There is only one phosphoenzyme intermediate with bound calcium on the reaction pathway of the sarcoplasmic reticulum calcium ATPase. Biochemistry. 34: 3077-83. PMID 7893720 DOI: 10.1021/bi00009a039 |
0.324 |
|
| 1995 |
Whitty A, Fierke CA, Jencks WP. Role of binding energy with coenzyme A in catalysis by 3-oxoacid coenzyme A transferase. Biochemistry. 34: 11678-89. PMID 7547900 DOI: 10.1021/Bi00037A005 |
0.753 |
|
| 1995 |
Eldin S, Jencks WP. Concerted bimolecular substitution reactions of anilino thioethers Journal of the American Chemical Society. 117: 9415-9418. DOI: 10.1021/Ja00142A005 |
0.371 |
|
| 1994 |
Simopoulos TT, Jencks WP. Alkaline phosphatase is an almost perfect enzyme. Biochemistry. 33: 10375-80. PMID 8068674 DOI: 10.1021/Bi00200A018 |
0.304 |
|
| 1994 |
Jencks WP. Reaction mechanisms, catalysis, and movement. Protein Science : a Publication of the Protein Society. 3: 2459-64. PMID 7757002 DOI: 10.1002/pro.5560031232 |
0.305 |
|
| 1993 |
Labow BI, Herschlag D, Jencks WP. Catalysis of the hydrolysis of phosphorylated pyridines by alkaline phosphatase has little or no dependence on the pKa of the leaving group. Biochemistry. 32: 8737-41. PMID 8395879 DOI: 10.1021/Bi00085A003 |
0.55 |
|
| 1993 |
Bednar RA, Jencks WP. Direct proton transfer between hydrocyanic acid and nitrogen and oxygen bases. [Erratum to document cited in CA103(25):214716g] Journal of the American Chemical Society. 115: 4947-4947. DOI: 10.1021/Ja00064A092 |
0.641 |
|
| 1993 |
Stefanidis D, Cho S, Dhe-Paganon S, Jencks WP. Structure-reactivity correlations for reactions of substituted phenolate anions with acetate and formate esters Journal of the American Chemical Society. 115: 1650-1656. DOI: 10.1021/Ja00058A006 |
0.397 |
|
| 1991 |
Banait NS, Jencks WP. Reactions of anionic nucleophiles with .alpha.-D-glucopyranosyl fluoride in aqueous solution through a concerted, ANDN (SN2) mechanism Journal of the American Chemical Society. 113: 7951-7958. DOI: 10.1021/Ja00021A021 |
0.309 |
|
| 1991 |
Berg U, Jencks WP. Does dissociation of amine water complexes depend upon amine basicity? Proton exchange between quinuclidinium ions and solvent Journal of the American Chemical Society. 113: 6997-7002. DOI: 10.1021/JA00018A043 |
0.302 |
|
| 1990 |
Herschlag D, Jencks WP. Catalysis of the hydrolysis of phosphorylated pyridines by Mg(OH)+: a possible model for enzymatic phosphoryl transfer. Biochemistry. 29: 5172-9. PMID 2378873 DOI: 10.1021/Bi00473A025 |
0.554 |
|
| 1990 |
Hanel AM, Jencks WP. Phosphorylation of the calcium-transporting adenosinetriphosphatase by lanthanum ATP: rapid phosphoryl transfer following a rate-limiting conformational change. Biochemistry. 29: 5210-20. PMID 2143081 DOI: 10.1021/Bi00473A030 |
0.318 |
|
| 1990 |
Banait NS, Jencks WP. Elimination reactions: Experimental confirmation of the predicted elimination of (β-cyanoethyl)sulfonium ions through a concerted, E2 mechanism Journal of the American Chemical Society. 112: 6950-6958. DOI: 10.1021/Ja00175A032 |
0.316 |
|
| 1990 |
Herschlag D, Jencks WP. Nucleophiles of high reactivity in phosphoryl transfer reactions: α-effect compounds and fluoride ion Journal of the American Chemical Society. 112: 1951-1956. DOI: 10.1021/Ja00161A047 |
0.56 |
|
| 1990 |
Herschlag D, Jencks WP. The effects of Mg2+, hydrogen bonding, and steric factors on rate and equilibrium constants for phosphoryl transfer between Carboxylate Ions and Pyridines Journal of the American Chemical Society. 112: 1942-1950. DOI: 10.1021/Ja00161A046 |
0.567 |
|
| 1990 |
HERSCHLAG D, JENCKS WP. ChemInform Abstract: Phosphoryl Transfer to Anionic Oxygen Nucleophiles. Nature of the Transition State and Electrostatic Repulsion. Cheminform. 21. DOI: 10.1002/CHIN.199001262 |
0.448 |
|
| 1989 |
Song BD, Jencks WP. Mechanism of solvolysis of substituted benzoyl halides Journal of the American Chemical Society®. 111: 8470-8479. DOI: 10.1021/Ja00204A021 |
0.323 |
|
| 1989 |
Amyes TL, Jencks WP. Concerted bimolecular substitution reactions of acetal derivatives of propionaldehyde and benzaldehyde Journal of the American Chemical Society. 111: 7900-7909. DOI: 10.1021/Ja00202A034 |
0.385 |
|
| 1989 |
Herschlag D, Jencks WP. Phosphoryl transfer to anionic oxygen nucleophiles. Nature of the transition state and electrostatic repulsion Journal of the American Chemical Society. 111: 7587-7596. DOI: 10.1021/Ja00201A048 |
0.581 |
|
| 1989 |
Herschlag D, Jencks WP. Evidence that metaphosphate monoanion is not an intermediate in solvolysis reactions in aqueous solution Journal of the American Chemical Society. 111: 7579-7586. DOI: 10.1021/Ja00201A047 |
0.571 |
|
| 1989 |
Dietze P, Jencks WP. Changes of selectivity in the reactions of substituted 4-nitrobenzyl sulfonates with nucleophilic reagents Journal of the American Chemical Society. 111: 5880-5886. DOI: 10.1021/Ja00197A057 |
0.35 |
|
| 1989 |
Washabaugh MW, Jencks WP. Thiazolium C(2)-proton exchange: General-base catalysis, direct proton transfer, and acid inhibition Journal of the American Chemical Society. 111: 674-683. DOI: 10.1021/Ja00184A042 |
0.33 |
|
| 1988 |
Chipman DM, Jencks WP. Specificity of the sarcoplasmic reticulum calcium ATPase at the hydrolysis step. Biochemistry. 27: 5707-12. PMID 2972313 DOI: 10.1021/Bi00415A047 |
0.369 |
|
| 1988 |
Washabaugh MW, Jencks WP. Thiazolium C(2)-proton exchange: structure-reactivity correlations and the pKa of thiamin C(2)-H revisited. Biochemistry. 27: 5044-53. PMID 2844248 DOI: 10.1021/Bi00414A015 |
0.335 |
|
| 1988 |
Murray CJ, Jencks WP. Proton-transfer reactions of sulfonium ylides: Unit Brønsted slopes do not require diffusion-controlled proton transfer Journal of the American Chemical Society. 110: 7561-7563. DOI: 10.1021/Ja00230A060 |
0.337 |
|
| 1988 |
Fishbein JC, Jencks WP. Elimination reactions of .beta.-cyano thioethers: evidence for a carbanion intermediate and a change in rate-limiting step Journal of the American Chemical Society. 110: 5075-5086. DOI: 10.1021/Ja00223A028 |
0.313 |
|
| 1987 |
Fishbein JC, Baum H, Cox MM, Jencks WP. Concerted general base and bifunctional general acid catalysis of the aminolysis of phenyl acetate by pyrazole Journal of the American Chemical Society. 109: 5790-5800. DOI: 10.1021/Ja00253A034 |
0.607 |
|
| 1987 |
Sørensen PE, Jencks WP. Acid- and base-catalyzed decomposition of acetaldehyde hydrate and hemiacetals in aqueous solution Journal of the American Chemical Society. 109: 4675-4690. DOI: 10.1021/Ja00249A034 |
0.319 |
|
| 1987 |
Herschlag D, Jencks WP. The effect of divalent metal ions on the rate and transition-state structure of phosphoryl-transfer reactions Journal of the American Chemical Society. 109: 4665-4674. DOI: 10.1021/Ja00249A033 |
0.543 |
|
| 1987 |
Dietze PE, Jencks WP. Oxygen exchange into 2-butanol and hydration of 1-butene do not proceed through a common carbocation intermediate Journal of the American Chemical Society. 109: 2057-2062. DOI: 10.1021/Ja00241A024 |
0.303 |
|
| 1987 |
HERSCHLAG D, JENCKS WP. ChemInform Abstract: The Effect of Divalent Metal Ions on the Rate and Transition-State Structure of Phosphoryl-Transfer Reactions. Cheminform. 18. DOI: 10.1002/CHIN.198746283 |
0.479 |
|
| 1987 |
HERSCHLAG D, JENCKS WP. ChemInform Abstract: Pyrophosphate Formation from Acetyl Phosphate and Orthophosphate Anions in Concentrated Aqueous Salt Solutions Does not Provide Evidence for a Metaphosphate Intermediate Cheminform. 18. DOI: 10.1002/CHIN.198717261 |
0.463 |
|
| 1986 |
Jencks WP, Haber MT, Herschlag D, Nazaretian KL. Decreasing reactivity with increasing nucleophile basicity. The effect of solvation on .beta.nuc for phosphoryl transfer to amines. Journal of the American Chemical Society. 108: 479-83. PMID 22175464 DOI: 10.1021/Ja00263A019 |
0.527 |
|
| 1986 |
Jencks WP, Haber MT, Herschlag D, Nazaretian KL. Additions and Corrections: Decreasing Reactivity with Increasing Nucleophile Basicity. The Effect of Solvation on (nuc) for Phosphoryl Transfer to Amines. Journal of the American Chemical Society. 108: 6100. PMID 22175415 DOI: 10.1021/Ja00279A603 |
0.525 |
|
| 1986 |
Fierke CA, Jencks WP. Two functional domains of coenzyme A activate catalysis by coenzyme A transferase. Pantetheine and adenosine 3'-phosphate 5'-diphosphate. The Journal of Biological Chemistry. 261: 7603-6. PMID 3458707 |
0.505 |
|
| 1986 |
Ta-Shma R, Jencks WP. How does a reaction change its mechanism? General base catalysis of the addition of alcohols to 1-phenylethyl carbocations Journal of the American Chemical Society. 108: 8040-8050. DOI: 10.1021/Ja00285A027 |
0.339 |
|
| 1986 |
Herschlag D, Jencks WP. Pyrophosphate formation from acetyl phosphate and orthophosphate anions in concentrated aqueous salt solutions does not provide evidence for a metaphosphate intermediate Journal of the American Chemical Society. 108: 7938-7946. DOI: 10.1021/Ja00285A010 |
0.566 |
|
| 1986 |
Dietze PE, Jencks WP. Swain-Scott correlations for reactions of nucleophilic reagents and solvents with secondary substrates Journal of the American Chemical Society. 108: 4549-4555. DOI: 10.1021/Ja00275A048 |
0.363 |
|
| 1986 |
Jencks WP, Haber MT, Herschlag D, Nazaretian KL. Decreasing reactivity with increasing nucleophile basicity. The effect of solvation on βnuc for phosphoryl transfer to amines Journal of the American Chemical Society. 108: 479-483. DOI: 10.1002/Chin.198623087 |
0.524 |
|
| 1985 |
Bednar RA, Jencks WP. Direct proton transfer between hydrocyanic acid and nitrogen and oxygen bases Journal of the American Chemical Society. 107: 7126-7134. DOI: 10.1021/Ja00310A061 |
0.631 |
|
| 1985 |
Bednar RA, Jencks WP. Is hydrocyanic acid a normal acid? Proton transfer from hydrocyanic acid to bases and small inhibition of proton exchange by acid Journal of the American Chemical Society. 107: 7117-7126. DOI: 10.1021/Ja00310A060 |
0.659 |
|
| 1985 |
Rothenberg ME, Richard JP, Jencks WP. Equilibrium constants for the interconversion of substituted 1-phenylethyl alcohols and ethers. A measurement of intramolecular electrostatic interactions Journal of the American Chemical Society. 107: 1340-1346. DOI: 10.1021/Ja00291A038 |
0.507 |
|
| 1985 |
Rothenberg ME, Richard JP, Jencks WP. Equilibrium constants for the interconversion of substituted 1-phenylethyl alcohols and ethers. A measurement of intramolecular electrostatic interactions Journal of the American Chemical Society. 107: 1340-1346. DOI: 10.1021/JA00291A038 |
0.437 |
|
| 1985 |
Bednar RA, Jencks WP. Intramolecular proton transfer through water in diamine monocations Journal of the American Chemical Society. 107: 7135-7138. DOI: 10.1002/Chin.198612156 |
0.633 |
|
| 1985 |
ROTHENBERG ME, RICHARD JP, JENCKS WP. ChemInform Abstract: EQUILIBRIUM CONSTANTS FOR THE INTERCONVERSION OF SUBSTITUTED 1-PHENYLETHYL ALCOHOLS AND ETHERS. A MEASUREMENT OF INTRAMOLECULAR ELECTROSTATIC INTERACTIONS Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198529093 |
0.444 |
|
| 1985 |
Bednar RA, Jencks WP. Is HCN a normal acid? Proton transfer from HCN to bases and small inhibition of proton exchange by acid Journal of the American Chemical Society. 107: 7117-7126. |
0.63 |
|
| 1985 |
Bednar RA, Jencks WP. Direct proton transfer between HCN and nitrogen and oxygen bases Journal of the American Chemical Society. 107: 7126-7134. |
0.605 |
|
| 1984 |
Pickart CM, Jencks WP. Energetics of the calcium-transporting ATPase. The Journal of Biological Chemistry. 259: 1629-43. PMID 6229538 |
0.656 |
|
| 1984 |
Richard JP, Jencks WP. General base catalysis of the addition of hydroxylic reagents to unstable carbocations and its disappearance Journal of the American Chemical Society. 106: 1396-1401. DOI: 10.1021/Ja00317A034 |
0.519 |
|
| 1984 |
Richard JP, Jencks WP. General base catalysis of the addition of hydroxylic reagents to unstable carbocations and its disappearance Journal of the American Chemical Society. 106: 1396-1401. DOI: 10.1021/JA00317A034 |
0.499 |
|
| 1984 |
Richard JP, Jencks WP. Concerted bimolecular substitution reactions of 1-phenylethyl derivatives Journal of the American Chemical Society. 106: 1383-1396. DOI: 10.1021/JA00317A033 |
0.525 |
|
| 1984 |
Richard JP, Jencks WP. Reactions of substituted 1-phenylethyl carbocations with alcohols and other nucleophilic reagents Journal of the American Chemical Society. 106: 1373-1383. DOI: 10.1021/JA00317A032 |
0.484 |
|
| 1984 |
Richard JP, Rothenberg ME, Jencks WP. Formation and stability of ring-substituted 1-phenylethyl carbocations Journal of the American Chemical Society. 106: 1361-1372. DOI: 10.1021/JA00317A031 |
0.455 |
|
| 1984 |
Skoog MT, Jencks WP. Reactions of pyridines and primary amines with N-phosphorylated pyridines Journal of the American Chemical Society. 106: 7597-7606. DOI: 10.1002/Chin.198512284 |
0.323 |
|
| 1984 |
RICHARD JP, JENCKS WP. ChemInform Abstract: GENERAL BASE CATALYSIS OF THE ADDITION OF HYDROXYLIC REAGENTS TO UNSTABLE CARBOCATIONS AND ITS DISAPPEARANCE Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198424095 |
0.505 |
|
| 1984 |
Richard JP, Jencks WP. Reactions of substituted 1-phenylethyl carbocations with alcohols and other nucleophilic reagents Journal of the American Chemical Society. 106: 1373-1383. DOI: 10.1002/Chin.198424094 |
0.54 |
|
| 1984 |
RICHARD JP, JENCKS WP. ChemInform Abstract: REACTIONS OF SUBSTITUTED 1-PHENYLETHYL CARBOCATIONS WITH ALCOHOLS AND OTHER NUCLEOPHILIC REAGENTS Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198424094 |
0.491 |
|
| 1984 |
Richard JP, Rothenberg ME, Jencks WP. Formation and stability of ring-substituted 1-phenylethyl carbocations Journal of the American Chemical Society. 106: 1361-1372. DOI: 10.1002/Chin.198424093 |
0.514 |
|
| 1984 |
RICHARD JP, ROTHENBERG ME, JENCKS WP. ChemInform Abstract: FORMATION AND STABILITY OF RING-SUBSTITUTED 1-PHENYLETHYL CARBOCATIONS Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198424093 |
0.464 |
|
| 1984 |
Richard JP, Jencks WP. Concerted bimolecular substitution reactions of 1-phenylethyl derivatives Journal of the American Chemical Society. 106: 1383-1396. DOI: 10.1002/Chin.198424089 |
0.576 |
|
| 1984 |
RICHARD JP, JENCKS WP. ChemInform Abstract: CONCERTED BIMOLECULAR SUBSTITUTION REACTIONS OF 1-PHENYLETHYL DERIVATIVES Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198424089 |
0.53 |
|
| 1983 |
Keefe J, Jencks W. Additions and Corrections - Elimination Reactions of N-(2-p-Nitrophenyl)ethyl) alkyl-ammonium Ions by an E1cB Mechanism Journal of the American Chemical Society. 105: 6195-6195. DOI: 10.1021/ja00357a601 |
0.34 |
|
| 1983 |
Keeffe JR, Jencks WP. Elimination reactions of N-(2-(p-nitrophenyl)ethyl)alkylammonium ions by an E1cB mechanism Journal of the American Chemical Society. 105: 265-279. DOI: 10.1021/Ja00340A021 |
0.326 |
|
| 1982 |
Pickart CM, Jencks WP. Slow dissociation of ATP from the calcium ATPase. The Journal of Biological Chemistry. 257: 5319-22. PMID 6461647 |
0.666 |
|
| 1982 |
Tapuhi E, Jencks WP. Base-catalyzed halogenation of acetone Journal of the American Chemical Society. 104: 5758-5765. DOI: 10.1021/Ja00385A034 |
0.333 |
|
| 1982 |
Richard JP, Jencks WP. Concerted SN2 displacement reactions of 1-phenylethyl chlorides Journal of the American Chemical Society. 104: 4691-4692. DOI: 10.1021/Ja00381A038 |
0.559 |
|
| 1982 |
Richard JP, Jencks WP. Concerted SN2 displacement reactions of 1-phenylethyl chlorides Journal of the American Chemical Society. 104: 4691-4692. DOI: 10.1021/JA00381A038 |
0.505 |
|
| 1982 |
Richard JP, Jencks WP. A simple relationship between carbocation lifetime and reactivity-selectivity relationships for the solvolysis of ring-substituted 1-phenylethyl derivatives Journal of the American Chemical Society. 104: 4689-4691. DOI: 10.1021/JA00381A037 |
0.448 |
|
| 1982 |
RICHARD JP, JENCKS WP. ChemInform Abstract: CONCERTED SN2 DISPLACEMENT REACTIONS OF 1-PHENYLETHYL CHLORIDES Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198247113 |
0.514 |
|
| 1982 |
Richard JP, Jencks WP. A simple relationship between carbocation lifetime and reactivity-selectivity relationships for the solvolysis of ring-substituted 1-phenylethyl derivatives Journal of the American Chemical Society. 104: 4689-4691. DOI: 10.1002/Chin.198247112 |
0.507 |
|
| 1982 |
RICHARD JP, JENCKS WP. ChemInform Abstract: A SIMPLE RELATIONSHIP BETWEEN CARBOCATION LIFETIME AND REACTIVITY-SELECTIVITY RELATIONSHIPS FOR THE SOLVOLYSIS OF RING-SUBSTITUTED 1-PHENYLETHYL DERIVATIVES Chemischer Informationsdienst. 13. DOI: 10.1002/CHIN.198247112 |
0.455 |
|
| 1982 |
Gandler JR, Jencks WP. General base catalysis, structure-reactivity interactions, and merging of mechanisms for elimination reactions of (2-arylethyl)quinuclidinium ions Journal of the American Chemical Society. 104: 1937-1951. DOI: 10.1002/Chin.198230106 |
0.342 |
|
| 1981 |
Cox MM, Jencks WP. Concerted bifunctional proton transfer and general-base catalysis in the methoxyaminolysis of phenyl acetate Journal of the American Chemical Society. 103: 580-587. DOI: 10.1021/Ja00393A014 |
0.548 |
|
| 1981 |
Cox MM, Jencks WP. Catalysis of the methoxyaminolysis of phenyl acetate by a preassociation mechanism with a solvent isotope effect maximum Journal of the American Chemical Society. 103: 572-580. DOI: 10.1021/Ja00393A013 |
0.584 |
|
| 1980 |
Levine L, Baer A, Jencks WP. Dissociation of pig liver carboxylesterase measured by quantitative micro-complement fixation. Archives of Biochemistry and Biophysics. 203: 236-43. PMID 7406500 DOI: 10.1016/0003-9861(80)90173-3 |
0.338 |
|
| 1980 |
Farb D, Jencks WP. Dependence on pH of the activity of pig liver esterase. Archives of Biochemistry and Biophysics. 203: 227-35. PMID 7406499 DOI: 10.1016/0003-9861(80)90172-1 |
0.607 |
|
| 1980 |
Farb D, Jencks WP. Different forms of pig liver esterase. Archives of Biochemistry and Biophysics. 203: 214-26. PMID 7406498 DOI: 10.1016/0003-9861(80)90171-X |
0.622 |
|
| 1980 |
Knier BL, Jencks WP. Mechanism of reactions of N-(methoxymethyl)-N,N-dimethylanilinium ions with nucleophilic reagents Journal of the American Chemical Society. 102: 6789-6798. DOI: 10.1021/Ja00542A021 |
0.334 |
|
| 1980 |
Palmer JL, Jencks WP. Secondary α-deuterium isotope effects for the cleavage of formaldehyde hemiacetals through concerted and specific-base-catalyzed pathways Journal of the American Chemical Society. 102: 6472-6481. DOI: 10.1021/JA00541A016 |
0.359 |
|
| 1980 |
Palmer JL, Jencks WP. Nonenforced concerted general-acid catalysis of the dehydration step in formaldehyde thiosemicarbazone formation Journal of the American Chemical Society. 102: 6466-6472. DOI: 10.1021/Ja00541A015 |
0.342 |
|
| 1980 |
Alunni S, Jencks WP. Catalysis of the reversible elimination reactions of substituted N-(.beta.-phenylethyl)quinuclidinium ions in aqueous solution Journal of the American Chemical Society. 102: 2052-2060. DOI: 10.1021/Ja00526A047 |
0.324 |
|
| 1980 |
Fischer H, DeCandis FX, Ogden SD, Jencks WP. Catalysis of transimination by rate-limiting proton transfer to buffer bases Journal of the American Chemical Society. 102: 1340-1347. DOI: 10.1021/Ja00524A018 |
0.339 |
|
| 1980 |
Alunni S, Jencks WP. Catalysis of the reversible elimination reactions of substituted N-(β-phenylethyl)quinuclidinium ions in aqueous solution Journal of the American Chemical Society. 102: 2052-2060. DOI: 10.1002/Chin.198025114 |
0.328 |
|
| 1979 |
Pickart CM, Jencks WP. Formation of stable anhydrides from CoA transferase and hydroxamic acids. The Journal of Biological Chemistry. 254: 9120-9. PMID 479182 |
0.695 |
|
| 1979 |
Reenstra WW, Jencks WP. Reactions of cyanide with cobalamins Journal of the American Chemical Society. 101: 5780-5791. DOI: 10.1021/Ja00513A052 |
0.347 |
|
| 1979 |
Thibblin A, Jencks WP. Unstable carbanions. General acid catalysis of the cleavage of 1-phenylcyclopropanol and 1-phenyl-2-arylcyclopropanol anions Journal of the American Chemical Society. 101: 4963-4973. DOI: 10.1021/Ja00511A028 |
0.349 |
|
| 1979 |
Thibblin A, Jencks WP. Unstable Carbanions. General Acid Catalysis Of The Cleavage Of 1‐Phenylcyclopropanol And 1‐Phenyl‐2‐Arylcyclopropanol Anions Cheminform. 10. DOI: 10.1002/Chin.197947113 |
0.34 |
|
| 1979 |
Young PR, Jencks WP. Separation of polar and resonance substituent effects in the reactions of acetophenones with bisulfite and of benzyl halides with nucleophiles Journal of the American Chemical Society. 101: 3288-3294. |
0.569 |
|
| 1978 |
Funderburk L, Jencks W. Additions and Corrections - Structure-Reactivity Coefficients for General Acid Catalysis of Semicarbazone Formation Journal of the American Chemical Society. 100: 8274-8274. DOI: 10.1021/JA00494A605 |
0.314 |
|
| 1978 |
Cox MM, Jencks WP. General acid catalysis of the aminolysis of phenyl acetate by a preassociation mechanism Journal of the American Chemical Society. 100: 5956-5957. DOI: 10.1021/Ja00486A065 |
0.549 |
|
| 1978 |
Funderburk LH, Jencks WP. Structure-reactivity coefficients for general acid catalysis of semicarbazone formation Journal of the American Chemical Society. 100: 6708-6714. DOI: 10.1002/Chin.197903091 |
0.312 |
|
| 1978 |
Cox MM, Jencks WP. General Acid Catalysis Of The Aminolysis Of Phenyl Acetate By A Preassociation Mechanism Cheminform. 9. DOI: 10.1002/Chin.197849135 |
0.549 |
|
| 1978 |
Funderburk LH, Aldwin L, Jencks WP. Mechanisms of general acid and base catalysis of the reactions of water and alcohols with formaldehyde Journal of the American Chemical Society. 100: 5444-5459. DOI: 10.1002/Chin.197848145 |
0.341 |
|
| 1978 |
Young PR, Jencks WP. General acid catalyzed breakdown of ketone bisulfites Journal of the American Chemical Society. 100: 1228-1235. |
0.58 |
|
| 1977 |
Hogg JL, Jencks DA, Jencks WP. Catalysis of transimination through trapping by acids and bases Journal of the American Chemical Society. 99: 4772-4778. DOI: 10.1021/Ja00456A039 |
0.303 |
|
| 1977 |
Young PR, Jencks WP. Nonenforced catalysis of the bisulfite carbonyl addition reaction by hydrogen bonding Journal of the American Chemical Society. 99: 1206-1214. |
0.555 |
|
| 1977 |
Young PR, Jencks WP. Trapping of the oxocarbonium ion intermediate in the hydrolysis of acetophenone dimethyl ketals Journal of the American Chemical Society. 99: 8238-8248. |
0.538 |
|
| 1976 |
White H, Solomon F, Jencks WP. Utilization of the inactivation rate of coenzyme A transferase by thiol reagents to determine properties of the enzyme-CoA intermediate. The Journal of Biological Chemistry. 251: 1700-7. PMID 1254595 |
0.53 |
|
| 1976 |
White H, Jencks WP. Mechanism and specificity of succinyl-CoA:3-ketoacid coenzyme A transferase. The Journal of Biological Chemistry. 251: 1688-99. PMID 1254594 |
0.304 |
|
| 1975 |
Jencks WP, Sayer JM. Structure and mechanism in complex general acid-base catalyzed reactions Faraday Symposia of the Chemical Society. 10: 41-49. DOI: 10.1039/FS9751000041 |
0.414 |
|
| 1974 |
Jencks WP, Page MI. "Orbital steering", entropy, and rate accelerations. Biochemical and Biophysical Research Communications. 57: 887-92. PMID 4827839 DOI: 10.1016/0006-291X(74)90629-9 |
0.324 |
|
| 1974 |
Satterthwait AC, Jencks WP. The mechanism of the aminolysis of acetate esters. Journal of the American Chemical Society. 96: 7018-31. PMID 4436508 DOI: 10.1021/Ja00829A034 |
0.301 |
|
| 1974 |
Williams A, Jencks WP. Acid and base catalysis of urea synthesis: Nonlinear brønsted plots consistent with a diffusion-controlled proton-transfer mechanism and the reactions of imidazole and N-methylimidazole with cyanic acid Journal of the Chemical Society, Perkin Transactions 2. 1760-1768. DOI: 10.1039/P29740001760 |
0.416 |
|
| 1974 |
Williams A, Jencks WP. Urea synthesis from amines and cyanic acid: Kinetic evidence for a zwitterionic intermediate Journal of the Chemical Society, Perkin Transactions 2. 1753-1759. DOI: 10.1039/P29740001753 |
0.4 |
|
| 1974 |
Satterthwait AC, Jencks WP. The mechanism of partitioning of the intermediates formed in the hydrolysis of phenyl imidates Journal of the American Chemical Society. 96: 7031-7044. DOI: 10.1021/Ja00829A035 |
0.328 |
|
| 1974 |
Gravitz N, Jencks WP. The mechanism of formation and breakdown of amine tetrahedral addition compounds of a phthalimidium cation. The relative leaving group abilities of amines and alkoxide ions Journal of the American Chemical Society. 96: 499-506. DOI: 10.1021/Ja00809A027 |
0.3 |
|
| 1974 |
Gravitz N, Jencks WP. Mechanism of hydrolysis of a phthalimidium cation. Direct observation and trapping of the tetrahedral addition intermediate and the effect of strong acid on rate and equilibrium constants of the reversible reaction Journal of the American Chemical Society. 96: 489-499. DOI: 10.1002/Chin.197414151 |
0.414 |
|
| 1973 |
Jencks WP, Farb D, Goldsmith L, Greenzaid P. Properties of pig liver esterase. Hoppe-Seyler's Zeitschrift Fã¼R Physiologische Chemie. 354: 2-3. PMID 4803238 |
0.52 |
|
| 1972 |
Page MI, Jencks WP. General base and acid catalysis in the hydrazinolysis of acetylimidazole Journal of the American Chemical Society. 94: 8828-8838. DOI: 10.1021/Ja00780A031 |
0.31 |
|
| 1972 |
Jencks WP. Requirements for general acid-base catalysis of complex reactions Journal of the American Chemical Society. 94: 4731-4732. DOI: 10.1021/Ja00768A052 |
0.368 |
|
| 1972 |
Fox JP, Page MI, Satterthwait A, Jencks WP. Nonlinear broensted relation for general acid-base catalysis of aminolysis reactions Journal of the American Chemical Society. 94: 4729-4731. DOI: 10.1021/JA00768A051 |
0.342 |
|
| 1971 |
Greenzaid P, Jencks WP. Pig liver esterase. Reactions with alcohols, structure-reactivity correlations, and the acyl-enzyme intermediate. Biochemistry. 10: 1210-22. PMID 5553326 DOI: 10.1021/Bi00783A018 |
0.313 |
|
| 1971 |
Page MI, Jencks WP. Entropic contributions to rate accelerations in enzymic and intramolecular reactions and the chelate effect. Proceedings of the National Academy of Sciences of the United States of America. 68: 1678-83. PMID 5288752 DOI: 10.1073/Pnas.68.8.1678 |
0.303 |
|
| 1971 |
Jencks WP, Salvesen K. Equilibrium deuterium isotope effects on the ionization of thiol acids Journal of the American Chemical Society. 93: 4433-4436. DOI: 10.1021/Ja00747A016 |
0.301 |
|
| 1971 |
Jencks WP, Salvesen K. The reaction of thiols with acetylimidazole. Evidence for independent reaction pathways Journal of the American Chemical Society. 93: 1419-1427. DOI: 10.1021/Ja00735A017 |
0.342 |
|
| 1971 |
Oakenfull DG, Salvesen K, Jencks WP. Reactions of acetylimidazole and acetylimidazolium ion with nucleophilic reagents. Mechanisms of catalysis Journal of the American Chemical Society. 93: 188-194. DOI: 10.1021/Ja00730A032 |
0.355 |
|
| 1971 |
Oakenfull DG, Jencks WP. Reactions of acetylimidazole and acetylimidazolium ion with nucleophilic reagents. Structure-reactivity relationships Journal of the American Chemical Society. 93: 178-188. DOI: 10.1021/Ja00730A031 |
0.335 |
|
| 1970 |
Fersht AR, Jencks WP. Reactions of nucleophilic reagents with acylating agents of extreme reactivity and unreactivity. Correlation of .beta. values for attacking and leaving group variation Journal of the American Chemical Society. 92: 5442-5452. DOI: 10.1021/Ja00721A024 |
0.591 |
|
| 1970 |
Fersht AR, Jencks WP. Acetylpyridinium ion intermediate in pyridine-catalyzed hydrolysis and acyl transfer reactions of acetic anhydride. Observation, kinetics, structure-reactivity correlations, and effects of concentrated salt solutions Journal of the American Chemical Society. 92: 5432-5442. DOI: 10.1021/Ja00721A023 |
0.645 |
|
| 1970 |
Jencks WP, Oakenfull DG, Salvesen K. Mechanism of general acid catalysis of the aminolysis of an amide Journal of the American Chemical Society. 92: 3201-3202. DOI: 10.1021/JA00713A056 |
0.326 |
|
| 1970 |
FERSHT AR, JENCKS WP. ChemInform Abstract: ACETYLPYRIDINIUMION-ZWISCHENPRODUKTE BEI DER DURCH PYRIDINE KATALYSIERTEN HYDROLYSE UND ACYLUEBERTRAGUNGSRK. VON ACETANHYDRID, BEOBACHTUNG, KINETIK, WECHSELBEZIEHUNG ZWISCHEN STRUKTUR UND REAKTIVITAET UND EFFEKTE VON KONZENTRIERTEN SA Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197047118 |
0.564 |
|
| 1970 |
BARNETT RE, JENCKS WP. ChemInform Abstract: DIFFUSIONSKONTROLLIERTE UND GLEICHLAUFENDE BASENKATALYSE BEI DER ZERS. VON HEMITHIOACETALEN Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197010080 |
0.579 |
|
| 1969 |
Solomon F, Jencks WP. Identification of an enzyme-gamma-glutamyl coenzyme A intermediate from coenzyme A transferase. The Journal of Biological Chemistry. 244: 1079-81. PMID 5769180 |
0.494 |
|
| 1969 |
Barnett RE, Jencks WP. Rates of hydrolysis of two thiol esters in water The Journal of Organic Chemistry. 34: 2777-2779. DOI: 10.1021/Jo01261A070 |
0.59 |
|
| 1969 |
Barnett RE, Jencks WP. Diffusion-controlled and concerted base catalysis in the decomposition of hemithioacetals Journal of the American Chemical Society. 91: 6758-6765. DOI: 10.1021/Ja01052A038 |
0.572 |
|
| 1969 |
Barnett RE, Jencks WP. Diffusion-controlled proton transfer in intramolecular thiol ester aminolysis and thiazoline hydrolysis Journal of the American Chemical Society. 91: 2358-2369. DOI: 10.1021/Ja01037A029 |
0.612 |
|
| 1969 |
Fersht AR, Jencks WP. Acetylpyridinium ion intermediate in pyridine-catalyzed acyl transfer Journal of the American Chemical Society. 91: 2125-2126. DOI: 10.1021/Ja01036A053 |
0.606 |
|
| 1968 |
St Pierre T, Jencks WP. Intramolecular catalysis in the reactions of nucleophilic reagents with aspirin. Journal of the American Chemical Society. 90: 3817-27. PMID 5653824 DOI: 10.1021/Ja01016A040 |
0.378 |
|
| 1968 |
Buchwald M, Jencks WP. Properties of the crustacyanins and the yellow lobster shell pigment. Biochemistry. 7: 844-59. PMID 5644143 DOI: 10.1021/Bi00842A043 |
0.522 |
|
| 1968 |
Buchwald M, Jencks WP. Optical properties of astaxanthin solutions and aggregates. Biochemistry. 7: 834-43. PMID 5644142 DOI: 10.1021/Bi00842A042 |
0.527 |
|
| 1968 |
Sander EG, Jencks WP. General acid and base catalysis of the reversible addition of hydrogen peroxide to aldehydes Journal of the American Chemical Society. 90: 4377-4386. DOI: 10.1021/JA01018A032 |
0.315 |
|
| 1967 |
Robinson DR, Jencks WP. Mechanism and catalysis of the hydrolysis of methenyltetrahydrofolic acid Journal of the American Chemical Society. 89: 7098-7103. DOI: 10.1021/JA01002A045 |
0.326 |
|
| 1967 |
Barnett RE, Jencks WP. Base-catalyzed hemithioacetal decomposition at a diffusion-controlled rate Journal of the American Chemical Society. 89: 5963-5964. DOI: 10.1021/Ja00999A047 |
0.588 |
|
| 1966 |
Lienhard GE, Jencks WP. Thiol addition to the carbonyl group. Equilibria and kinetics. Journal of the American Chemical Society. 88: 3982-94. PMID 5915153 DOI: 10.1021/Ja00969A017 |
0.555 |
|
| 1966 |
Jencks WP, Barley F, Barnett R, Gilchrist M. The free energy of hydrolysis of acetic anhydride. Journal of the American Chemical Society. 88: 4464-7. PMID 5912570 |
0.54 |
|
| 1965 |
Lienhard GE, Jencks WP. The reaction of carbanions with N,S-diacetylcysteamine. A model for enzymatic carbon--carbon condensation. Journal of the American Chemical Society. 87: 3863-74. PMID 5845265 DOI: 10.1021/Ja01095A013 |
0.542 |
|
| 1965 |
Lienhard GE, Jencks WP. Kinetic Demonstration of a Tetrahedral Intermediate in the Hydrolysis of Diethyl Acetylmalonate and Diethyl Acetylethylmalonate1 Journal of the American Chemical Society. 87: 3855-3862. DOI: 10.1021/Ja01095A012 |
0.608 |
|
| 1965 |
Kirby AJ, Jencks WP. Base Catalysis of the Reaction of Secondary Amines with p-Nitrophenyl Phosphate. Kinetic Evidence for an Addition Intermediate in Nucleophilic Aromatic Substitution1 Journal of the American Chemical Society. 87: 3217-3224. DOI: 10.1021/ja01092a037 |
0.633 |
|
| 1965 |
Kirby AJ, Jencks WP. The Reactivity of Nucleophilic Reagents toward the p-Nitrophenyl Phosphate Dianion1 Journal of the American Chemical Society. 87: 3209-3216. DOI: 10.1021/ja01092a036 |
0.572 |
|
| 1965 |
Jencks WP, Gilchrist M. Reactions of Nucleophilic Reagents with Phosphoramidate1 Journal of the American Chemical Society. 87: 3199-3209. DOI: 10.1021/JA01092A035 |
0.359 |
|
| 1964 |
Jencks WP, Gilchrist M. The Reaction of Hydroxylamine with Amides. Kinetic Evidence for the Existence of a Tetrahedral Addition Intermediate Journal of the American Chemical Society. 86: 5616-5620. DOI: 10.1021/JA01078A042 |
0.378 |
|
| 1964 |
Gerstein J, Jencks WP. Equilibria and Rates for Acetyl Transfer among Substituted Phenyl Acetates, Acetylimidazole, O-Acylhydroxamic Acids, and Thiol Esters Journal of the American Chemical Society. 86: 4655-4663. DOI: 10.1021/JA01075A027 |
0.33 |
|
| 1964 |
Jencks WP, Gilchrist M. Electrophilic Catalysis. The Hydrolysis of Phosphoramidate Journal of the American Chemical Society. 86: 1410-1417. DOI: 10.1021/JA01061A029 |
0.388 |
|
| 1964 |
Kirsch JF, Jencks WP. Nonlinear Structure-Reactivity Correlations. The Imidazole-Catalyzed Hydrolysis of Esters Journal of the American Chemical Society. 86: 837-846. DOI: 10.1021/Ja01059A019 |
0.518 |
|
| 1964 |
Kirsch JF, Jencks WP. Base Catalysis of Imidazole Catalysis of Ester Hydrolysis Journal of the American Chemical Society. 86: 833-837. DOI: 10.1021/Ja01059A018 |
0.579 |
|
| 1963 |
JENCKS WP, CAPLOW M, GILCHRIST M, KALLEN RG. EQUILIBRIUM CONSTANTS FOR THE SYNTHESIS OF HYDROXAMIC ACIDS. Biochemistry. 2: 1313-20. PMID 14093907 DOI: 10.1021/Bi00906A024 |
0.307 |
|
| 1963 |
Cordes EH, Jencks WP. The mechanism of hydrolysis of Schiff bases derived from aliphatic amines Journal of the American Chemical Society. 85: 2843-2848. |
0.56 |
|
| 1962 |
CORDES EH, JENCKS WP. Semicarbazone formation from pyridoxal, pyridoxal phosphate, and their Schiff bases. Biochemistry. 1: 773-8. PMID 14022996 |
0.544 |
|
| 1962 |
CAPLOW M, JENCKS WP. The effect of substituents on the deacylation of benzoyl-chymotrypsins. Biochemistry. 1: 883-93. PMID 14018421 DOI: 10.1021/Bi00911A022 |
0.761 |
|
| 1962 |
Sabato GD, Jencks WP, Whalley E. THE EFFECT OF PRESSURE ON THE SPONTANEOUS HYDROLYSIS OF ACETYL PHOSPHATE MONO-ANION AND DI-ANION AND OF ACETYL PHENYL PHOSPHATE MONO-ANION Canadian Journal of Chemistry. 40: 1220-1224. DOI: 10.1139/V62-186 |
0.301 |
|
| 1962 |
Hand ES, Jencks WP. Mechanism of the Reaction of Imido Esters with Amines Journal of the American Chemical Society. 84: 3505-3514. DOI: 10.1021/JA00877A017 |
0.377 |
|
| 1962 |
Cordes EH, Jencks WP. Nucleophilic catalysis of semicarbazone formation by anilines Journal of the American Chemical Society. 84: 826-831. DOI: 10.1021/Ja00864A030 |
0.611 |
|
| 1962 |
Cordes EH, Jencks WP. On the mechanism of Schiff base formation and hydrolysis Journal of the American Chemical Society. 84: 832-837. |
0.544 |
|
| 1962 |
Cordes EH, Jencks WP. General acid catalysis of semicarbazone formation Journal of the American Chemical Society. 84: 4319-4328. |
0.553 |
|
| 1961 |
ANDERSON BM, CORDES EH, JENCKS WP. Reactivity and catalysis in reactions of the serine hydroxyl group and of O-acyl serines. The Journal of Biological Chemistry. 236: 455-63. PMID 13683176 |
0.556 |
|
| 1961 |
Di Sabato G, Jencks WP. Mechanism and Catalysis of Reactions of Acyl Phosphates. II. Hydrolysis1 Journal of the American Chemical Society. 83: 4400-4405. DOI: 10.1021/JA01482A025 |
0.342 |
|
| 1961 |
Di Sabato G, Jencks WP. Mechanism and Catalysis of Reactions of Acyl Phosphates. I. Nucleophilic Reactions1 Journal of the American Chemical Society. 83: 4393-4400. DOI: 10.1021/JA01482A024 |
0.389 |
|
| 1961 |
Wolfenden R, Jencks WP. Acetyl Transfer Reactions of 1-Acetyl-3-methylimidazolium Chloride1 Journal of the American Chemical Society. 83: 4390-4393. DOI: 10.1021/JA01482A023 |
0.347 |
|
| 1961 |
Wolfenden R, Jencks WP. The Effect of o-Substituents on Benzaldehyde Semicarbazone Formation1 Journal of the American Chemical Society. 83: 2763-2768. DOI: 10.1021/Ja01473A037 |
0.608 |
|
| 1960 |
Jencks WP, Carriuolo J. Reactivity of Nucleophilic Reagents toward Esters Journal of the American Chemical Society. 82: 1778-1786. DOI: 10.1021/JA01492A058 |
0.355 |
|
| 1958 |
Jencks WP. The Reaction of Hydroxylamine with Activated Acyl Groups. II. Mechanism of the Reaction Journal of the American Chemical Society. 80: 4585-4588. DOI: 10.1021/JA01550A041 |
0.34 |
|
| 1958 |
Jencks WP. The Reaction of Hydroxylamine with Activated Acyl Groups. I. Formation of O-Acylhydroxylamine1 Journal of the American Chemical Society. 80: 4581-4584. DOI: 10.1021/JA01550A040 |
0.311 |
|
| 1957 |
JENCKS WP, LIPMANN F. Studies on the initial step of fatty acid activation. The Journal of Biological Chemistry. 225: 207-23. PMID 13416231 |
0.607 |
|
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