| Year |
Citation |
Score |
| 2020 |
Costa PFA, de Abreu R, Fontana AB, Fiedler HD, Kirby AJ, Quina FH, Nome F, Gerola AP. The role of hydrophobicity in supramolecular polymer/surfactant catalysts: An understandable model for enzymatic catalysis. Journal of Colloid and Interface Science. 588: 456-468. PMID 33429342 DOI: 10.1016/j.jcis.2020.12.081 |
0.512 |
|
| 2017 |
Gerola AP, Wanderlind EH, Gomes YS, Giusti LA, García-Río L, Nome RA, Kirby AJ, Fiedler HD, Nome F. Supramolecular Polymer/Surfactant Complexes as Catalysts for Phosphate Transfer Reactions Acs Catalysis. 7: 2230-2239. DOI: 10.1021/Acscatal.7B00097 |
0.566 |
|
| 2015 |
Kirby AJ, Nome F. Fundamentals of Phosphate Transfer. Accounts of Chemical Research. PMID 26075464 DOI: 10.1021/Acs.Accounts.5B00072 |
0.608 |
|
| 2015 |
Komarov IV, Yanik S, Ishchenko AY, Davies JE, Goodman JM, Kirby AJ. The most reactive amide as a transition-state mimic for cis-trans interconversion. Journal of the American Chemical Society. 137: 926-30. PMID 25533746 DOI: 10.1021/Ja511460A |
0.327 |
|
| 2015 |
Kirby AJ, Souza BS, Nome F. Structure and reactivity of phosphate diesters. Dependence on the nonleaving group Canadian Journal of Chemistry. 93: 422-427. DOI: 10.1139/Cjc-2014-0358 |
0.606 |
|
| 2015 |
Aldersley MF, Joshi PC, Ott EL, McCallum SA, Kirby AJ. The introduction of P-F bonds using aqueous fluoride ion and a water soluble carbodiimide: a convenient alternative synthesis of phosphorofluoridates and phosphonofluoridates Tetrahedron Letters. 56: 5272-5274. DOI: 10.1016/J.Tetlet.2015.07.036 |
0.346 |
|
| 2014 |
Ishchenko AY, Yanik S, Rusanov EB, Komarov IV, Kirby AJ. An expedient and practical approach to functionalized 3-aza-, 3-oxa-, and 3-thiabicyclo[33.1]nonane systems Synthesis (Germany). 46. DOI: 10.1055/S-0034-1379456 |
0.368 |
|
| 2014 |
Aldersley MF, Joshi PC, Schwartz HM, Kirby AJ. The reaction of activated RNA species with aqueous fluoride ion: A convenient synthesis of nucleotide 5′-phosphorofluoridates and a note on the mechanism Tetrahedron Letters. 55: 1464-1466. DOI: 10.1016/J.Tetlet.2014.01.051 |
0.38 |
|
| 2013 |
Medeiros M, Wanderlind EH, Mora JR, Moreira R, Kirby AJ, Nome F. Major mechanistic differences between the reactions of hydroxylamine with phosphate di- and tri-esters. Organic & Biomolecular Chemistry. 11: 6272-84. PMID 23900489 DOI: 10.1039/C3Ob40988K |
0.603 |
|
| 2013 |
Kirby AJ, Medeiros M, Mora JR, Oliveira PS, Amer A, Williams NH, Nome F. Intramolecular general base catalysis in the hydrolysis of a phosphate diester. Calculational guidance to a choice of mechanism. The Journal of Organic Chemistry. 78: 1343-53. PMID 23373989 DOI: 10.1021/Jo302498G |
0.711 |
|
| 2013 |
Kirby AJ, Mora JR, Nome F. New light on phosphate transfer from triesters. Biochimica Et Biophysica Acta. 1834: 454-63. PMID 22575086 DOI: 10.1016/J.Bbapap.2012.04.010 |
0.607 |
|
| 2013 |
Medeiros M, Manfredi AM, Kirby AJ, Nome F. The spontaneous hydrolysis of 2-pyridyl phosphate is a good model for the special mechanism for the hydrolysis of phosphate monoester monoanions Journal of Physical Organic Chemistry. 26: 1044-1047. DOI: 10.1002/Poc.3165 |
0.61 |
|
| 2012 |
Medeiros M, Orth ES, Manfredi AM, Pavez P, Micke GA, Kirby AJ, Nome F. Dephosphorylation reactions of mono-, di-, and triesters of 2,4-dinitrophenyl phosphate with deferoxamine and benzohydroxamic acid. The Journal of Organic Chemistry. 77: 10907-13. PMID 23167539 DOI: 10.1021/Jo302374Q |
0.624 |
|
| 2012 |
Mora JR, Kirby AJ, Nome F. Theoretical study of the importance of the spectator groups on the hydrolysis of phosphate triesters. The Journal of Organic Chemistry. 77: 7061-70. PMID 22835036 DOI: 10.1021/Jo301380V |
0.59 |
|
| 2012 |
Babtie AC, Lima MF, Kirby AJ, Hollfelder F. Kinetic and computational evidence for an intermediate in the hydrolysis of sulfonate esters. Organic & Biomolecular Chemistry. 10: 8095-101. PMID 22832951 DOI: 10.1039/C2Ob25699A |
0.646 |
|
| 2012 |
Delley RJ, Bandyopadhyay S, Fox MA, Schliehe C, Hodgson DR, Hollfelder F, Kirby AJ, O'Donoghue AC. peri-Dimethylamino substituent effects on proton transfer at carbon in α-naphthylacetate esters: a model for mandelate racemase. Organic & Biomolecular Chemistry. 10: 590-6. PMID 22108698 DOI: 10.1039/C1Ob06525D |
0.698 |
|
| 2012 |
Orth ES, Medeiros M, Souza BS, Caon NB, Kirby AJ, Nome F. Reactions of substituted aspirins with amino acids Journal of Physical Organic Chemistry. 25: 939-945. DOI: 10.1002/Poc.2971 |
0.615 |
|
| 2011 |
Kirby AJ, Medeiros M, Oliveira PS, Orth ES, Brandão TA, Wanderlind EH, Amer A, Williams NH, Nome F. Activating water: important effects of non-leaving groups on the hydrolysis of phosphate triesters. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 14996-5004. PMID 22106028 DOI: 10.1002/Chem.201101926 |
0.715 |
|
| 2011 |
Orth ES, Medeiros M, Bortolotto T, Terenzi H, Kirby AJ, Nome F. Dephosphorylation reactions with deferoxamine, a potential chemical nuclease. The Journal of Organic Chemistry. 76: 10345-8. PMID 22049907 DOI: 10.1021/Jo202074Y |
0.574 |
|
| 2011 |
Orth ES, Wanderlind EH, Medeiros M, Oliveira PS, Vaz BG, Eberlin MN, Kirby AJ, Nome F. Phosphorylimidazole derivatives: potentially biosignaling molecules. The Journal of Organic Chemistry. 76: 8003-8. PMID 21861472 DOI: 10.1021/Jo2017394 |
0.507 |
|
| 2011 |
Medeiros M, Souza BS, Orth ES, Brandão TAS, Rocha W, Kirby AJ, Nome F. The reaction of hydroxylamine with aspirin Arkivoc. 2011: 461-476. DOI: 10.3998/Ark.5550190.0012.738 |
0.609 |
|
| 2010 |
Souza BS, Vitto R, Nome F, Kirby AJ, Bortoluzzi AJ. 3-Acet-oxy-2-naphthoic acid. Acta Crystallographica. Section E, Structure Reports Online. 66: o2848. PMID 21589033 DOI: 10.1107/S1600536810040365 |
0.553 |
|
| 2010 |
Orth ES, Brandão TA, Souza BS, Pliego JR, Vaz BG, Eberlin MN, Kirby AJ, Nome F. Intramolecular catalysis of phosphodiester hydrolysis by two imidazoles. Journal of the American Chemical Society. 132: 8513-23. PMID 20509675 DOI: 10.1021/Ja1034733 |
0.589 |
|
| 2010 |
Kirby AJ, Davies JE, Fox DJ, Hodgson DR, Goeta AE, Lima MF, Priebe JP, Santaballa JA, Nome F. Ammonia oxide makes up some 20% of an aqueous solution of hydroxylamine. Chemical Communications (Cambridge, England). 46: 1302-4. PMID 20449284 DOI: 10.1039/B923742A |
0.499 |
|
| 2010 |
Kirby AJ, Marriott RE. Rapid intramolecular and C-O cleavage reactions of a phosphate triester catalysed by a neighbouring hydroxyl group Recueil Des Travaux Chimiques Des Pays-Bas. 115: 56-62. DOI: 10.1002/Recl.19961150111 |
0.429 |
|
| 2010 |
Wagenaar A, Kirby AJ, Engberts JBFN. Acid-catalyzed hydrolysis of benzenesulfonamides. Rate enhancements by ortho-alkyl substituents Recueil Des Travaux Chimiques Des Pays-Bas. 104: 203-205. DOI: 10.1002/Recl.19851040704 |
0.369 |
|
| 2010 |
Hollfelder F, Kirby AJ, Tawfik DS, Kikuchi K, Hilvert D. ChemInform Abstract: Characterization of Proton-Transfer Catalysis by Serum Albumins Cheminform. 31: no-no. DOI: 10.1002/chin.200018038 |
0.493 |
|
| 2009 |
Kirby AJ, Medeiros M, Oliveira PS, Brandão TA, Nome F. Activating water: efficient intramolecular general base catalysis of the hydrolysis of a phosphate triester. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 8475-9. PMID 19621399 DOI: 10.1002/Chem.200901096 |
0.58 |
|
| 2009 |
Kirby AJ, Tondo DW, Medeiros M, Souza BS, Priebe JP, Lima MF, Nome F. Efficient intramolecular general-acid catalysis of the reactions of alpha-effect nucleophiles and ammonia oxide with a phosphate triester. Journal of the American Chemical Society. 131: 2023-8. PMID 19159237 DOI: 10.1021/Ja808746F |
0.581 |
|
| 2009 |
Kirby AJ, Manfredi AM, Souza BS, Medeiros M, Priebe JP, Brandão TAS, Nome F. Reactions of alpha-nucleophiles with a model phosphate diester Arkivoc. 2009: 28-38. DOI: 10.3998/Ark.5550190.0010.305 |
0.585 |
|
| 2009 |
Iddon L, Bragg RA, Harding JR, Pidathala C, Bacsa J, Kirby AJ, Stachulski AV. Syntheses and structures of anomeric quaternary ammonium β-glucosides and comments on the anomeric C-N bond lengths Tetrahedron. 65: 6396-6402. DOI: 10.1016/J.Tet.2009.05.086 |
0.339 |
|
| 2008 |
Kirby AJ, Hollfelder F. Biochemistry: Enzymes under the nanoscope. Nature. 456: 45-7. PMID 18987728 DOI: 10.1038/456045A |
0.556 |
|
| 2008 |
Kirby AJ, Souza BS, Medeiros M, Priebe JP, Manfredi AM, Nome F. Hydroxylamine as an oxygen nucleophile. Chemical evidence from its reaction with a phosphate triester. Chemical Communications (Cambridge, England). 4428-9. PMID 18802579 DOI: 10.1039/B810408E |
0.575 |
|
| 2007 |
Ferreira VBN, Bortoluzzi AJ, Kirby AJ, Nome F. 2-Allyloxy-5-chlorobenzoic acid Acta Crystallographica Section E: Structure Reports Online. 63: o2981. DOI: 10.1107/S1600536807024762 |
0.538 |
|
| 2007 |
Kirby A. Enzymatic Reaction Mechanisms. By Perry A. Frey and Adrian D. Hegeman. Angewandte Chemie International Edition. 46: 7922-7924. DOI: 10.1002/Anie.200785514 |
0.327 |
|
| 2007 |
Kirby A. Enzymatic Reaction Mechanisms. Von Perry A. Frey und Adrian D. Hegeman. Angewandte Chemie. 119: 8068-8070. DOI: 10.1002/Ange.200785514 |
0.327 |
|
| 2006 |
Kirby AJ, Lima MF, da Silva D, Roussev CD, Nome F. Efficient intramolecular general acid catalysis of nucleophilic attack on a phosphodiester. Journal of the American Chemical Society. 128: 16944-52. PMID 17177446 DOI: 10.1021/Ja066439U |
0.626 |
|
| 2006 |
Kirby AJ, Davies JE, Brandão TA, da Silva PF, Rocha WR, Nome F. Hydroxylamine as an oxygen nucleophile. Structure and reactivity of ammonia oxide. Journal of the American Chemical Society. 128: 12374-5. PMID 16984161 DOI: 10.1021/Ja065147Q |
0.533 |
|
| 2005 |
Kirby AJ, Dutta-Roy N, da Silva D, Goodman JM, Lima MF, Roussev CD, Nome F. Intramolecular general acid catalysis of phosphate transfer. nucleophilic attack by oxyanions on the PO3 2- group. Journal of the American Chemical Society. 127: 7033-40. PMID 15884947 DOI: 10.1021/Ja0502876 |
0.641 |
|
| 2005 |
Kirby AJ, Gesser JC, Hollfelder F, Priebe JP, Nome F. Intramolecular general acid catalysis of sulfate transfer - Nucleophilic attack by oxyanions on the so3 - group Canadian Journal of Chemistry. 83: 1629-1636. DOI: 10.1139/v05-172 |
0.697 |
|
| 2005 |
Brandão TAS, Priebe JP, Damasceno AS, Bortoluzzi AJ, Kirby AJ, Nome F. Bond length-reactivity correlations for sulfate monoesters. The crystal structure of potassium 4-nitrophenyl sulfate, C 6H 4KNO 6S Journal of Molecular Structure. 734: 205-209. DOI: 10.1016/J.Molstruc.2004.09.025 |
0.551 |
|
| 2005 |
Asaad N, Davies JE, Hodgson DRW, Kirby AJ, Van Vliet L, Ottavi L. The search for efficient intramolecular proton transfer from carbon: The kinetically silent intramolecular general base-catalysed elimination reaction of O-phenyl 8-dimethylamino-1-naphthaldoximes Journal of Physical Organic Chemistry. 18: 101-109. DOI: 10.1002/Poc.858 |
0.398 |
|
| 2004 |
Kaneti J, Kirby AJ, Koedjikov AH, Pojarlieff IG. Thorpe-Ingold effects in cyclizations to five-membered and six-membered rings containing planar segments. The rearrangement of N(1)-alkyl-substituted dihydroorotic acids to hydantoinacetic acids in base. Organic & Biomolecular Chemistry. 2: 1098-103. PMID 15034636 DOI: 10.1039/B400248B |
0.41 |
|
| 2004 |
Kirby AJ, Lima MF, da Silva D, Nome F. Nucleophilic attack by oxyanions on a phosphate monoester dianion: the positive effect of a cationic general Acid. Journal of the American Chemical Society. 126: 1350-1. PMID 14759187 DOI: 10.1021/Ja038428W |
0.616 |
|
| 2004 |
Blériot Y, Vadivel SK, Herrera AJ, Greig IR, Kirby AJ, Sinaÿ P. Synthesis and acid catalyzed hydrolysis of B2,5 type conformationally constrained glucopyranosides: Incorporation into a cellobiose analogue Tetrahedron. 60: 6813-6828. DOI: 10.1016/J.Tet.2004.06.009 |
0.34 |
|
| 2004 |
Greig IR, Kirby AJ. Free energy relationships and intramolecular general acid catalysis Journal of Physical Organic Chemistry. 17: 498-506. DOI: 10.1002/Poc.766 |
0.398 |
|
| 2003 |
Angelova VT, Kirby AJ, Koedjikov AH, Pojarlieff IG. Kinetics and mechanism of the cyclization of omega-(p-nitrophenyl)-hydantoic acid amides: steric hindrance to proton transfer causes a 10(4)-fold change in rate. Organic & Biomolecular Chemistry. 1: 859-65. PMID 12929371 DOI: 10.1039/B211040G |
0.476 |
|
| 2003 |
Davies JE, Kirby AJ, Komarov IV. Structural correlations for nucleophilic addition to the C=O group: The solvation angle Helvetica Chimica Acta. 86: 1222-1233. DOI: 10.1002/Hlca.200390105 |
0.38 |
|
| 2003 |
Kirby AJ. Thermodynamics of Biochemical Reactions. By Robert A. Alberty. Angewandte Chemie International Edition. 42: 4428-4428. DOI: 10.1002/Anie.200385024 |
0.347 |
|
| 2002 |
Kirby AJ, Komarov IV, Bilenko VA, Davies JE, Rawson JM. Structure and chemistry of a zwitterionic amine-aldehyde adduct. Chemical Communications (Cambridge, England). 2106-7. PMID 12357800 DOI: 10.1039/B206639D |
0.326 |
|
| 2002 |
Davies JE, Doltsinis NL, Kirby AJ, Roussev CD, Sprik M. Estimating pKa values for pentaoxyphosphoranes. Journal of the American Chemical Society. 124: 6594-9. PMID 12047179 DOI: 10.1021/Ja025779M |
0.315 |
|
| 2002 |
Jones PG, Kirby AJ, Pilkington M. 2,2,2-Tris(cyclohexyloxy)-4,5-(2′,2′'-biphenylo)-1,3,2-dioxaphospholene Acta Crystallographica Section E Structure Reports Online. 58: o268-o269. DOI: 10.1107/S1600536802002398 |
0.309 |
|
| 2002 |
Asaad N, Kirby AJ. Concurrent nucleophilic and general acid catalysis of the hydrolysis of a phosphate triester Journal of the Chemical Society, Perkin Transactions 2. 1708-1712. DOI: 10.1039/B204609A |
0.475 |
|
| 2002 |
Ronsin G, Kirby AJ, Rittenhouse S, Woodnutt G, Camilleri P. Structure and antimicrobial activity of new bile acid-based gemini surfactants Journal of the Chemical Society, Perkin Transactions 2. 1302-1306. DOI: 10.1039/B202552C |
0.35 |
|
| 2002 |
Dean KES, Kirby AJ. Concerted general acid and nucleophilic catalysis of acetal hydrolysis. A simple model for the lysozyme mechanism Journal of the Chemical Society, Perkin Transactions 2. 428-432. DOI: 10.1039/B110948K |
0.448 |
|
| 2002 |
Kirby AJ, Marriott RE. General base catalysis vs. medium effects in the hydrolysis of an RNA model Journal of the Chemical Society, Perkin Transactions 2. 422-427. DOI: 10.1039/B109325H |
0.384 |
|
| 2002 |
Dean KES, Kirby AJ, Komarov IV. Torsional effects on reactivity in glycosyl transfer Journal of the Chemical Society, Perkin Transactions 2. 337-341. DOI: 10.1039/B106257N |
0.347 |
|
| 2001 |
Bond AD, Kirby AJ, Rodriguez E. Efficient intramolecular general acid catalysis: a preview from a crystal structure. Chemical Communications (Cambridge, England). 2266-7. PMID 12240143 DOI: 10.1039/B107787B |
0.373 |
|
| 2001 |
Hollfelder F, Kirby AJ, Tawfik DS. On the magnitude and specificity of medium effects in enzyme-like catalysts for proton transfer. The Journal of Organic Chemistry. 66: 5866-74. PMID 11511264 DOI: 10.1021/Jo015723V |
0.606 |
|
| 2001 |
Kirby AJ, Wothers PD. Conformational equilibria involving 2-amino-1,3-dioxans: Steric control of the anomeric effect Arkivoc. 2001: 58-71. DOI: 10.3998/Ark.5550190.0002.C07 |
0.368 |
|
| 2000 |
Kirby AJ, Hollfelder F, Tawfik DS. Nonspecific catalysis by protein surfaces. Applied Biochemistry and Biotechnology. 83: 173-80; discussion 1. PMID 10826958 DOI: 10.1385/Abab:83:1-3:173 |
0.598 |
|
| 2000 |
Pérez-Juste J, Hollfelder F, Kirby AJ, Engberts JB. Vesicles accelerate proton transfer from carbon up to 850-fold. Organic Letters. 2: 127-30. PMID 10814263 DOI: 10.1021/Ol991215K |
0.546 |
|
| 2000 |
Blagoeva IB, Kirby AJ, Kochiyashki II, Koedjikov AH, Pojarlieff IG, Toteva MM. A normal gem-dimethyl effect in the base-catalyzed cyclization of ω-(p-nitrophenyl)hydantoic acids: evidence for hindered proton transfer in the permethylated esters Journal of the Chemical Society-Perkin Transactions 1. 1953-1960. DOI: 10.1039/B002276O |
0.457 |
|
| 2000 |
Hollfelder F, Kirby AJ, Tawfik DS, Kikuchi K, Hilvert D. Characterization of proton-transfer catalysis by serum albumins Journal of the American Chemical Society. 122: 1022-1029. DOI: 10.1021/Ja993471Y |
0.614 |
|
| 2000 |
Hartwell E, Hodgson DRW, Kirby AJ. Exploring the Limits of Efficiency of Proton-Transfer Catalysis in Models and Enzymes Journal of the American Chemical Society. 122: 9326-9327. DOI: 10.1021/Ja002335M |
0.313 |
|
| 1999 |
Kirby AJ, Komarov IV, Wothers PD, Feeder N, Jones PG. Stereoelectronic interactions between hetero-atoms Pure and Applied Chemistry. 71: 385-391. DOI: 10.1351/Pac199971030385 |
0.333 |
|
| 1999 |
Barber SE, Dean KE, Kirby AJ. A mechanism for efficient proton-transfer catalysis. Intramolecular general acid catalysis of the hydrolysis of 1-arylethyl ethers of salicylic acid Canadian Journal of Chemistry. 77: 792-801. DOI: 10.1139/V99-080 |
0.464 |
|
| 1999 |
Blagoeva IB, Kirby AJ, Koedjikov AH, Pojarlieff IG. Multiple changes in rate-determining step in the acid and base catalyzed cyclizations of ethyl N-(p-nitrophenyl)hydantoates caused by methyl substitution Canadian Journal of Chemistry. 77: 849-859. DOI: 10.1139/V99-079 |
0.438 |
|
| 1999 |
Kirby AJ, Komarov IV, Kowski K, Rademacher P. Distortion of the amide bond in amides and lactams. Photoelectron-spectrum and electronic structure of 3,5,7-trimethyl-1-azaadamantan-2-one, the most twisted amide Journal of the Chemical Society-Perkin Transactions 1. 1313-1316. DOI: 10.1039/A902321F |
0.307 |
|
| 1998 |
Kirby AJ, Komarov IV, Wothers PD, Feeder N. The Most Twisted Amide: Structure and Reactions. Angewandte Chemie (International Ed. in English). 37: 785-786. PMID 29711382 DOI: 10.1002/(Sici)1521-3773(19980403)37:6<785::Aid-Anie785>3.0.Co;2-J |
0.374 |
|
| 1998 |
Atay E, Blagoeva IB, Kirby AJ, Pojarlieff IG. On the disappearance of the gem-dimethyl effect: the base-catalysed cyclization of ethyl hydantoates† Journal of the Chemical Society-Perkin Transactions 1. 2289-2298. DOI: 10.1039/A802884B |
0.451 |
|
| 1998 |
Tickle D, George A, Jennings K, Camilleri P, Kirby AJ. A study of the structure and chiral selectivity of micelles of two isomeric D-glucopyranoside-based surfactants Journal of the Chemical Society-Perkin Transactions 1. 467-474. DOI: 10.1039/A708418H |
0.332 |
|
| 1998 |
Beckmann C, Kirby AJ, Kuusela S, Tickle DC. Mechanisms of catalysis by imidazole buffers of the hydrolysis and isomerisation of RNA models Journal of the Chemical Society-Perkin Transactions 1. 573-582. DOI: 10.1039/A707741F |
0.46 |
|
| 1998 |
Kirby AJ, Komarov IV, Feeder N. Spontaneous, Millisecond Formation of a Twisted Amide from the Amino Acid, and the Crystal Structure of a Tetrahedral Intermediate Journal of the American Chemical Society. 120: 7101-7102. DOI: 10.1021/Ja980700S |
0.343 |
|
| 1998 |
Kirby A, Komarov I, Wothers P, Feeder N. Struktur und Reaktionen von 3,6,9-Trimethyl-1-aza-2-adamantanon, dem am stärksten verdrillten Amid Angewandte Chemie. 110: 830-831. DOI: 10.1002/(Sici)1521-3757(19980316)110:6<830::Aid-Ange830>3.0.Co;2-K |
0.313 |
|
| 1997 |
Deslongchamps P, Jones PG, Li S, Kirby AJ, Kuusela S, Ma Y. Stereoelectronic effects on reactivity. Crystal-structure–reactivity correlations for acetals with synperiplanar lone pairs Journal of the Chemical Society-Perkin Transactions 1. 2621-2626. DOI: 10.1039/A705142E |
0.383 |
|
| 1997 |
Brown CJ, Kirby AJ. Efficiency of proton transfer catalysis. Intramolecular general acid catalysis of the hydrolysis of dialkyl acetals of benzaldehyde Journal of the Chemical Society-Perkin Transactions 1. 1081-1094. DOI: 10.1039/A700155J |
0.448 |
|
| 1997 |
Genre-Grandpierre A, Tellier C, Loirat M, Blanchard D, Hodgson DR, Hollfelder F, Kirby AJ. Catalysis of the Kemp elimination by antibodies elicited against a cationic hapten Bioorganic & Medicinal Chemistry Letters. 7: 2497-2502. DOI: 10.1016/S0960-894X(97)10003-8 |
0.586 |
|
| 1996 |
Capasso S, Mazzarella L, Sorrentino G, Balboni G, Kirby AJ. Kinetics and mechanism of the cleavage of the peptide bond next to asparagine. Peptides. 17: 1075-7. PMID 8899829 DOI: 10.1016/0196-9781(96)00153-2 |
0.409 |
|
| 1996 |
Hollfelder F, Kirby AJ, Tawfik DS. Off-the-shelf proteins that rival tailor-made antibodies as catalysts. Nature. 383: 60-2. PMID 8779715 DOI: 10.1038/383060A0 |
0.572 |
|
| 1996 |
Koedjikov AH, Blagoeva IB, Pojarlieff IG, Kirby AJ. The gem-dimethyl effect on reactivities in cyclizations through tetrahedral intermediates. Cyclization of methyl-substituted methyl amides of 5-(p-nitrophenyl)hydantoic acids Journal of the Chemical Society-Perkin Transactions 1. 2479-2487. DOI: 10.1039/P29960002479 |
0.456 |
|
| 1996 |
Brown CJ, Kirby AJ. Efficient intramolecular general acid catalysis of the hydrolysis of a dialkyl acetal Chemical Communications. 2355-2356. DOI: 10.1039/Cc9960002355 |
0.456 |
|
| 1996 |
Kirby AJ. Enzyme Mechanisms, Models, and Mimics Angewandte Chemie International Edition in English. 35: 706-724. DOI: 10.1002/Anie.199607061 |
0.327 |
|
| 1995 |
Bedford CT, Kirby AJ, Logan CJ, Drummond JN. Structure-activity studies of sulfate transfer: the hydrolysis and aminolysis of 3'-phosphoadenosine 5'-phosphosulfate (PAPS). Bioorganic & Medicinal Chemistry. 3: 167-72. PMID 7796050 DOI: 10.1016/0968-0896(95)00015-9 |
0.371 |
|
| 1995 |
Al-Lohedan HA, Kirby AJ. Solvent effects on aromatic nucleophilic substitution by the ANRORC mechanism. Hydrolysis of 2-chloro-3,5-dinitropyridine Journal of the Chemical Society-Perkin Transactions 1. 1283-1286. DOI: 10.1039/P29950001283 |
0.336 |
|
| 1995 |
Capasso S, Kirby AJ, Salvadori S, Sica F, Zagari A. Kinetics and mechanism of the reversible isomerization of aspartic acid residues in tetrapeptides Journal of the Chemical Society-Perkin Transactions 1. 437-442. DOI: 10.1039/P29950000437 |
0.415 |
|
| 1994 |
Dalby KN, Kirby AJ, Hollfelder F. Simple but efficient models for nuclease catalysis Pure and Applied Chemistry. 66: 687-694. DOI: 10.1351/Pac199466040687 |
0.779 |
|
| 1994 |
Camilleri P, Jones RFD, Kirby AJ, Strömberg R. Nucleophilic catalysis of glycoside hydrolysis. The hydrolysis of 4-nitrophenyl α- and β-D-glucopyranoside tetraphosphates Journal of the Chemical Society-Perkin Transactions 1. 2085-2090. DOI: 10.1039/P29940002085 |
0.365 |
|
| 1994 |
Kirby AJ, O'Carroll F. Highly efficient intramolecular general acid catalysis of enol ether hydrolysis, with rapid proton transfer to carbon Journal of the Chemical Society-Perkin Transactions 1. 649-655. DOI: 10.1039/P29940000649 |
0.433 |
|
| 1994 |
Kirby AJ, Williams NH. Efficient intramolecular general acid catalysis of enol ether hydrolysis. Hydrogen-bonding stabilisation of the transition state for proton transfer to carbon Journal of the Chemical Society, Perkin Transactions 2. 643-648. DOI: 10.1039/P29940000643 |
0.63 |
|
| 1994 |
Chandler AJ, Hollfelder F, Kirby AJ, O'Carroll F, Strömberg R. Models for enzyme-catalysed phosphate transfer: comparisons of reactivity towards a neighbouring hydroxy group for phosphodiester anions and acids. General base catalysis of the cyclisation of a hydroxyalkyl phosphate triester Journal of the Chemical Society-Perkin Transactions 1. 327-333. DOI: 10.1039/P29940000327 |
0.653 |
|
| 1994 |
Jones RFD, Camilleri P, Kirby AJ, Okafo GN. The synthesis and micellar properties of a novel anionic surfactant Journal of the Chemical Society, Chemical Communications. 1311-1312. DOI: 10.1039/C39940001311 |
0.321 |
|
| 1994 |
Kirby AJ, Strömberg R. Intramolecular nucleophilic catalysis of glucoside hydrolysis by the 2-phosphate group Journal of the Chemical Society, Chemical Communications. 709-710. DOI: 10.1039/C39940000709 |
0.378 |
|
| 1994 |
Kirby AJ, Parkinson A. Most efficient intramolecular general acid catalysis of acetal hydrolysis by the carboxy group Journal of the Chemical Society, Chemical Communications. 707-708. DOI: 10.1039/C39940000707 |
0.441 |
|
| 1993 |
Dalby KN, Kirby AJ, Hollfelder F. Models for nuclease catalysis: Mechanisms for general acid catalysis of the rapid intramolecular displacement of methoxide from a phosphate diester Journal of the Chemical Society-Perkin Transactions 1. 1269-1281. DOI: 10.1039/P29930001269 |
0.679 |
|
| 1992 |
Jones PG, Kirby AJ, Parker JK. Bond length and reactivity. The effect of β-silicon. Structure of the 3,5-dinitrobenzoate ester of trans-2-(dimethylphenylsilyl)cyclohexanol Acta Crystallographica Section C Crystal Structure Communications. 48: 868-871. DOI: 10.1107/S0108270191012283 |
0.316 |
|
| 1992 |
Jones PG, Kirby AJ, Parker JK. Bond length and reactivity. The effect of β-fluorine. Structure of the methanesulfonate ester of trans,trans-5-tert-butyl-2-fluorocyclohexanol Acta Crystallographica Section C Crystal Structure Communications. 48: 864-866. DOI: 10.1107/S010827019101226X |
0.303 |
|
| 1992 |
Jones PG, Kirby AJ, Parker JK. Bond length and reactivity. The effect of β-fluorine. Structures of the 9-(9-phenylxanthenyl) ether, and the 4-phenylbenzoate, diphenyl phosphate and methanesulfonate esters of cis,trans-4-tert-butyl-2-fluorocyclohexanol Acta Crystallographica Section C Crystal Structure Communications. 48: 859-864. DOI: 10.1107/S0108270191012258 |
0.342 |
|
| 1992 |
Jones PG, Kirby AJ, Parker JK. Bond length and reactivity. The effect of β-fluorine. Structures of the 4-phenylbenzoate and methanesulfonate esters of trans,cis-4-tert-butyl-2-fluorocyclohexanol Acta Crystallographica Section C Crystal Structure Communications. 48: 855-858. DOI: 10.1107/S0108270191012246 |
0.318 |
|
| 1992 |
Kirby AJ, Parker JK, Raithby PR. Bond length and reactivity. Structure of 2-phenylethyl p-toluenesulfonate Acta Crystallographica Section C Crystal Structure Communications. 48: 832-834. DOI: 10.1107/S0108270191012167 |
0.301 |
|
| 1992 |
Jones PG, Schmidt-Bäse K, Edwards MR, Kirby AJ. Bond length and reactivity. Structure of 2-endo-bornyl p-toluenesulfonate Acta Crystallographica Section C Crystal Structure Communications. 48: 826-829. DOI: 10.1107/S0108270191012143 |
0.306 |
|
| 1992 |
Amos RD, Handy NC, Jones PG, Kirby AJ, Parker JK, Percy JM, Der Su M. Bond length and reactivity: The gauche effect. A combined crystallographic and theoretical investigation of the effects of β-substituents on C-OX bond length Journal of the Chemical Society, Perkin Transactions 2. 549-558. DOI: 10.1039/P29920000549 |
0.34 |
|
| 1992 |
Dalby KN, Hollfelder F, Kirby AJ. Electrostatic catalysis of the hydrolysis of a phosphate diester in water Journal of the Chemical Society, Chemical Communications. 1770-1771. DOI: 10.1039/C39920001770 |
0.763 |
|
| 1992 |
Chandler AJ, Kirby AJ. Intramolecular attack by the hydroxy group on phosphate diesters is both general acid and general base catalysed Journal of the Chemical Society, Chemical Communications. 1769-1770. DOI: 10.1039/C39920001769 |
0.445 |
|
| 1992 |
Kirby AJ, Williams NH. The anomeric effects of aryloxy groups Journal of the Chemical Society, Chemical Communications. 1286-1287. DOI: 10.1039/C39920001286 |
0.533 |
|
| 1992 |
Kirby AJ, Williams NH. Electronic effects on conformational preferences: A-values for aryloxy groups Journal of the Chemical Society, Chemical Communications. 1285-1286. DOI: 10.1039/C39920001285 |
0.527 |
|
| 1991 |
Kirby AJ, Williams NH. There is no evidence for electrostatic catalysis of vinyl ether hydrolysis in water Journal of the Chemical Society, Chemical Communications. 1644-1645. DOI: 10.1039/C39910001644 |
0.616 |
|
| 1991 |
Kirby AJ, Williams NH. Efficient intramolecular general acid catalysis of vinyl ether hydrolysis by the neighbouring carboxylic acid group Journal of the Chemical Society, Chemical Communications. 1643-1644. DOI: 10.1039/C39910001643 |
0.621 |
|
| 1990 |
Kirby AJ, Ryder H, Matassa V. Stabilisation of the thromboxane ring system by electron-withdrawing substituents. Mechanism and reactivity in the hydrolysis of alkyl and aryl oxetane acetals Journal of the Chemical Society-Perkin Transactions 1. 825-831. DOI: 10.1039/P29900000825 |
0.413 |
|
| 1990 |
Kirby AJ, Ryder H, Matassa V. Stabilisation of the thromboxane ring system by electron-withdrawing substituents: synthesis and attempted cyclisation of substituted tetrahydropyran-2,4-diols Journal of the Chemical Society-Perkin Transactions 1. 617-626. DOI: 10.1039/P19900000617 |
0.34 |
|
| 1989 |
Jones PG, Edwards MR, Kirby AJ. Bond length and reactivity. The pinacol rearrangement. 4. Structures of trans-2-hydroxycyclohexyl benzenesulfonate, p-toluenesulfonate and 2-naphthalenesulfonate Acta Crystallographica Section C Crystal Structure Communications. 45: 252-257. DOI: 10.1107/S0108270188011333 |
0.32 |
|
| 1989 |
Jones PG, Edwards MR, Kirby AJ. Bond length and reactivity. The pinacol rearrangement. 3. Structures of trans-2-hydroxycyclohexyl 4-nitrobenzoate and 2,4-dinitrobenzoate esters Acta Crystallographica Section C Crystal Structure Communications. 45: 249-252. DOI: 10.1107/S0108270188011321 |
0.347 |
|
| 1989 |
Jones PG, Edwards MR, Kirby AJ. Bond length and reactivity. The pinacol rearrangement. 1. Redetermination of the structure of trans-cyclohexane-1,2-diol Acta Crystallographica Section C Crystal Structure Communications. 45: 244-247. DOI: 10.1107/S010827018801131X |
0.328 |
|
| 1989 |
Jones PG, Edwards MR, Kirby AJ. Bond length and reactivity. The pinacol rearrangement. 2. Structure of trans-2-phenoxycyclohexanol Acta Crystallographica Section C Crystal Structure Communications. 45: 247-249. DOI: 10.1107/S0108270188011308 |
0.321 |
|
| 1989 |
Jones PG, Kirby AJ, Ryder H. Bond length and reactivity. Structure of 2-(4-nitrophenoxy)tetrahydrofuran Acta Crystallographica Section C Crystal Structure Communications. 45: 239-241. DOI: 10.1107/S010827018801128X |
0.303 |
|
| 1989 |
Jones PG, Kirby AJ, Parker JK. Bond length and reactivity: 1-arylethyl ethers and esters. 7. Structure of 1-[3,5-bis(trifluoromethyl)phenyl]ethyl 4-nitrobenzoate Acta Crystallographica Section C Crystal Structure Communications. 45: 218-221. DOI: 10.1107/S0108270188010200 |
0.366 |
|
| 1989 |
Jones PG, Schmidt-Bäse K, Kirby AJ, Parker JK. Bond length and reactivity. Structures of the triphenylmethyl ethers of 1-indanol and 5-methoxy-1-indanol Acta Crystallographica Section C Crystal Structure Communications. 45: 221-224. DOI: 10.1107/S0108270188010194 |
0.319 |
|
| 1989 |
Kirby AJ, Parker JK, Raithby PR. Bond length and reactivity. Structure of 1-indanol 4-nitrobenzoate ester Acta Crystallographica Section C Crystal Structure Communications. 45: 224-226. DOI: 10.1107/S0108270188010182 |
0.331 |
|
| 1989 |
Jones PG, Kirby AJ, Parker JK. Bond length and reactivity. Structure of 3,5-bis(trifluoromethyl)benzyl 4-nitrobenzoate Acta Crystallographica Section C Crystal Structure Communications. 45: 237-239. DOI: 10.1107/S0108270188010145 |
0.327 |
|
| 1989 |
Kirby AJ, Percy JM. Intramolecular proton-transfer catalysis of nucleophilic catalysis of acetal hydrolysis. The hydrolysis of 8-dimethylamino-1-methoxymethoxynaphthalene Journal of the Chemical Society-Perkin Transactions 1. 907-912. DOI: 10.1039/P29890000907 |
0.435 |
|
| 1989 |
Blagoeva IB, Pojarlieff IG, Tashev DT, Kirby AJ. Intramolecular nucleophilic attack by urea nitrogen. Reactivity–selectivity relationships for the general acid–base catalysed cyclisations of ureido acids and esters Journal of the Chemical Society-Perkin Transactions 1. 347-353. DOI: 10.1039/P29890000347 |
0.464 |
|
| 1988 |
Amyes TL, Kirby AJ. Intramolecular nucleophilic addition of phenolate oxygen to double bonds activated by carboxyl and carboxylate groups. Relative reactivity, stereochemistry, and mechanism Journal of the American Chemical Society. 110: 6505-6514. DOI: 10.1021/Ja00227A035 |
0.404 |
|
| 1988 |
Kirby AJ, Percy JM. Exceptional reactivity of the aromatic ring in 8-substituted 1-naphthol derivatives. Ready reduction to tetralins Tetrahedron. 44: 6911-6919. DOI: 10.1016/S0040-4020(01)86221-9 |
0.312 |
|
| 1988 |
Kirby AJ, Percy JM. Synthesis of 8-substituted 1-naphthylamine derivatives. exceptional reactivity of the substituents. Tetrahedron. 44: 6903-6910. DOI: 10.1016/S0040-4020(01)86220-7 |
0.327 |
|
| 1987 |
Edwards MR, Kirby AJ, Raithby PR, Jones PG. Bond length and reactivity: the Beckmann rearrangement. 5. Structure of 4-phenylcyclohexanone oxime O-4-nitrobenzoate ester at 290 K Acta Crystallographica Section C Crystal Structure Communications. 43: 300-303. DOI: 10.1107/S0108270187096057 |
0.309 |
|
| 1987 |
Barber SE, Kirby AJ. Intramolecular proton transfer catalysis of ether hydrolysis Journal of the Chemical Society, Chemical Communications. 1775-1776. DOI: 10.1039/C39870001775 |
0.462 |
|
| 1987 |
Kirby AJ, Percy JM. The hydrogen bond as a key factor in efficient intramolecular proton transfer catalysis Journal of the Chemical Society, Chemical Communications. 1774-1775. DOI: 10.1039/C39870001774 |
0.388 |
|
| 1986 |
Jones PG, Sheldrick GM, Edwards MR, Kirby AJ. Bond length and reactivity: 1-arylethyl ethers and esters. 3. Structures of three trityl ethers of 1-arylethanols: 1-phenylethyl, 1-(4-chlorophenyl)ethyl and 1-(4-nitrophenyl)ethyl triphenylmethyl ethers Acta Crystallographica Section C Crystal Structure Communications. 42: 1361-1364. DOI: 10.1107/S0108270186092260 |
0.369 |
|
| 1986 |
Drummond JN, Kirby AJ. Intramolecular catalysis of sulphate diester hydrolysis by one and two carboxy groups. The hydrolysis of aryl 2-carboxyphenyl sulphates Journal of the Chemical Society-Perkin Transactions 1. 579-583. DOI: 10.1039/P29860000579 |
0.471 |
|
| 1986 |
Abell KW, Kirby AJ. Acceleration of P-O cleavage reactions of phosphate monoester dianions in dipolar aprotic solvents Tetrahedron Letters. 27: 1085-1088. DOI: 10.1016/S0040-4039(86)80055-7 |
0.374 |
|
| 1985 |
Jones PG, Sheldrick GM, Kirby AJ, Briggs AJ. Bond length and reactivity. Structure of 1-methoxymethoxy-3,5-dinitrobenzene, C8H8N2O6 Acta Crystallographica Section C Crystal Structure Communications. 41: 1377-1379. DOI: 10.1107/S0108270185007843 |
0.303 |
|
| 1985 |
WAGENAAR A, KIRBY AJ, ENGBERTS JBFN. ChemInform Abstract: ACID-CATALYZED HYDROLYSIS OF BENZENESULFONAMIDES. RATE ENHANCEMENTS BY ORTHO-ALKYL SUBSTITUENTS Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198551083 |
0.407 |
|
| 1985 |
Wagenaar A, Kirby AJ, Engberts JBFN. Intramolecularly Catalyzed Sulfonamide Hydrolysis. 8. Intramolecular Nucleophilic Catalysis By A Neighboring Hydroxyl Group In Acid-Catalyzed Benzenesulfonamide Hydrolysis Cheminform. 16. DOI: 10.1002/Chin.198509225 |
0.483 |
|
| 1984 |
Jones PG, Sheldrick GM, Kirby AJ, Abell KWY. Bis(cyclohexylammonium) propargyl phosphate dihydrate, 2C6H14N+.C3H3O4P2−.2H2O Acta Crystallographica Section C Crystal Structure Communications. 40: 547-549. DOI: 10.1107/S0108270184004819 |
0.304 |
|
| 1984 |
Jones PG, Sheldrick GM, Kirby AJ, Briggs AJ. 2-Methoxymethoxybenzoic acid, C9H10O4 Acta Crystallographica Section C Crystal Structure Communications. 40: 545-547. DOI: 10.1107/S0108270184004807 |
0.318 |
|
| 1984 |
Evans CM, Kirby AJ. Intramolecular nucleophilic addition of phenolate to unactivated double and triple bonds. Relative reactivity, regiospecificity, stereochemistry, and mechanism Journal of the Chemical Society, Perkin Transactions 2. 1269-1275. DOI: 10.1039/P29840001269 |
0.437 |
|
| 1984 |
Evans CM, Kirby AJ. A model for olefin hydration: Intramolecular nucleophilic addition of phenolate oxygen to the unactivated double bond Journal of the Chemical Society, Perkin Transactions 2. 1259-1267. DOI: 10.1039/P29840001259 |
0.452 |
|
| 1984 |
Blagoeva IB, Pojarlieff IG, Kirby AJ. Intramolecular nucleophilic attack on carboxylate by ureide anion. General acid–base catalysis of the alkaline cyclisation of 2,2,3,5-tetramethylhydantoic acid Journal of the Chemical Society-Perkin Transactions 1. 15: 745-751. DOI: 10.1039/P29840000745 |
0.478 |
|
| 1984 |
Wagenaar A, Kirby AJ, Engberts JBFN. Intramolecular-Catalyzed Sulfonamide Hydrolysis .8. Intramolecular Nucleophilic Catalysis By The Neighboring Hydroxyl Group In Acid-Catalyzed Benzenesulfonamide Hydrolysis Journal of Organic Chemistry. 49: 3445-3448. DOI: 10.1021/Jo00193A001 |
0.419 |
|
| 1984 |
Kirby AJ. Stereoelectronic effects on acetal hydrolysis Accounts of Chemical Research. 17: 305-311. DOI: 10.1021/Ar00105A002 |
0.349 |
|
| 1984 |
Jones PG, Kirby AJ. Simple correlation between bond length and reactivity. Combined use of crystallographic and kinetic data to explore a reaction coordinate Journal of the American Chemical Society. 106: 6207-6212. DOI: 10.1002/Chin.198506059 |
0.364 |
|
| 1984 |
Briggs AJ, Glenn R, Jones PG, Kirby AJ, Ramaswamy P. Bond length and reactivity. Stereoelectronic effects on bonding in acetals and glucosides Journal of the American Chemical Society. 106: 6200-6206. DOI: 10.1002/Chin.198506058 |
0.301 |
|
| 1984 |
Jager J, Graafland T, Schenk H, Kirby AJ, Engberts JBFN. Intramolecular-Catalyzed Sulfonamide Hydrolysis. Vii. The Thorpe-Ingold Effect In The Intramolecular Carboxyl-Catalyzed Hydrolysis Of Sulfonamides Cheminform. 15. DOI: 10.1002/Chin.198416151 |
0.319 |
|
| 1983 |
Briggs AJ, Evans CM, Glenn R, Kirby AJ. Stereoelectronic effects at oxygen. A very large effect on the hydrolysis of a conformationally locked acetal: Implications for β-glycosidase mechanisms Journal of the Chemical Society, Perkin Transactions 2. 1637-1640. DOI: 10.1039/P29830001637 |
0.343 |
|
| 1983 |
Kirby AJ, Martin RJ. Stereoelectronic effects on acetal cleavage. The separation of the π-donor and σ-acceptor properties of oxygen Journal of the Chemical Society-Perkin Transactions 1. 15: 1633-1636. DOI: 10.1039/P29830001633 |
0.363 |
|
| 1983 |
Kirby AJ, Martin RJ. Stereoelectronic control of the hydrolysis of a conformationally locked acetal Journal of the Chemical Society-Perkin Transactions 1. 15: 1627-1632. DOI: 10.1039/P29830001627 |
0.441 |
|
| 1983 |
Chandrasekhar S, Kirby AJ, Martin RJ. Stereoelectronic effects at oxygen. The hydrolysis of 2-aryloxy-trans-1-oxadecalins Journal of the Chemical Society-Perkin Transactions 1. 15: 1619-1626. DOI: 10.1039/P29830001619 |
0.375 |
|
| 1983 |
Abell KWY, Kirby AJ. Intramolecular general acid catalysis of intramolecular nucleophilic catalysis of the hydrolysis of a phosphate diester Journal of the Chemical Society-Perkin Transactions 1. 14: 1171-1174. DOI: 10.1039/P29830001171 |
0.466 |
|
| 1983 |
ABELL KWY, KIRBY AJ. ChemInform Abstract: INTRAMOLECULAR GENERAL ACID CATALYSIS OF INTRAMOLECULAR NUCLEOPHILIC CATALYSIS OF THE HYDROLYSIS OF A PHOSPHATE DIESTER Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198348140 |
0.345 |
|
| 1982 |
Jones PG, Kirby AJ. Evidence from crystal structures for an incipient fragmentation reaction Journal of the Chemical Society, Chemical Communications. 1365-1366. DOI: 10.1039/C39820001365 |
0.31 |
|
| 1981 |
Graafland T, Kirby AJ, Engberts JBFN. Intramolecular carboxyl-catalyzed hydrolysis of sulfonamides. 5. Salt effects on the intramolecular carboxyl-catalyzed hydrolysis of sulfonamides The Journal of Organic Chemistry. 46: 215-217. DOI: 10.1021/Jo00314A059 |
0.461 |
|
| 1981 |
Graafland T, Kirby AJ, Engberts JBFN. Intramolecular Carboxyl-Catalyzed Hydrolysis Of Sulfonamides. 5. Salt Effects S On The Intramolecular Carboxyl-Catalyzed Hydrolysis Of Sulfonamides Cheminform. 12. DOI: 10.1002/Chin.198124169 |
0.433 |
|
| 1980 |
Graafland T, Wagenaar A, Kirby A, Engberts J. Additions and Corrections - Structure and Reactivity in Intramolecular Catalysis. Catalysis of Sulfonamide Hydrolysis by the Neighboring Carboxyl Group Journal of the American Chemical Society. 102: 3663-3663. DOI: 10.1021/Ja00530A606 |
0.429 |
|
| 1980 |
Graafland T, Wagenaar A, Kirby AJ, Engberts JBFN. Structure And Reactivity In Intramolecular Catalysis. Catalysis Of Sulfonamide Hydrolysis By The Neighboring Carboxyl Group Cheminform. 11. DOI: 10.1002/Chin.198007173 |
0.362 |
|
| 1979 |
Camilleri P, Ellul R, Kirby AJ, Mujahid TG. The spontaneous formation of amides. The mechanism of lactam formation from 3-(2-aminophenyl)propionic acid Journal of the Chemical Society-Perkin Transactions 1. 11: 1617-1620. DOI: 10.1039/P29790001617 |
0.401 |
|
| 1979 |
Kirby AJ, Mujahid TG, Camilleri P. Anilide formation from an aliphatic ester. The mechanism of cyclisation of methyl 3-(2-aminophenyl)propionate Journal of the Chemical Society-Perkin Transactions 1. 11: 1610-1616. DOI: 10.1039/P29790001610 |
0.447 |
|
| 1979 |
Jones PG, Kirby AJ. Linear relationship between bond length and reactivity Journal of the Chemical Society, Chemical Communications. 288-289. DOI: 10.1039/C39790000288 |
0.349 |
|
| 1979 |
CAMILLERI P, CASSOLA A, KIRBY AJ, MUJAHID TG. ChemInform Abstract: NUCLEOPHILIC ATTACK BY AMINE NITROGEN ON THE IONIZED CARBOXY GROUP Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197904181 |
0.371 |
|
| 1978 |
Craze G, Kirby AJ, Osborne R. Bimolecular nucleophilic substitution on an acetal Journal of the Chemical Society-Perkin Transactions 1. 9: 357-368. DOI: 10.1039/P29780000357 |
0.455 |
|
| 1978 |
Camilleri P, Cassola A, Kirby AJ, Mujahid TG. Nucleophilic attack by amine nitrogen on the ionised carboxy group Journal of the Chemical Society, Chemical Communications. 807-808. DOI: 10.1039/C39780000807 |
0.43 |
|
| 1978 |
Kirby AJ, Martin RJ. Stereoelectronic control of acetal hydrolysis Journal of the Chemical Society, Chemical Communications. 803-804. DOI: 10.1039/C39780000803 |
0.346 |
|
| 1978 |
Kirby AJ, Mujahid TG. Intramolecular nucleophilic catalysis of amide hydrolysis by pyrimidine nitrogen Tetrahedron Letters. 19: 4081-4084. DOI: 10.1016/S0040-4039(01)95146-9 |
0.447 |
|
| 1976 |
Kirby AJ, Lloyd GJ. The E1cb mechanism for ester hydrolysis. Evidence for a dianion intermediate in the hydrolysis of aryl malonate anions Journal of the Chemical Society-Perkin Transactions 1. 8: 1762-1768. DOI: 10.1039/P29760001762 |
0.476 |
|
| 1976 |
Kirby AJ, Lloyd GJ. Structure and efficiency in intramolecular and enzymic catalysis: intramolecular general base catalysis. Hydrolysis of monoaryl malonates Journal of the Chemical Society-Perkin Transactions 1. 8: 1753-1761. DOI: 10.1039/P29760001753 |
0.413 |
|
| 1976 |
Kirby AJ, Lloyd GJ. Intramolecular general base catalysis in the hydrolysis of 3-dimethylaminopropionates Journal of the Chemical Society-Perkin Transactions 1. 8: 1748-1752. DOI: 10.1039/P29760001748 |
0.456 |
|
| 1975 |
WAGENAAR A, KIRBY AJ, ENGBERTS JBFN. ChemInform Abstract: INTRAMOLECULAR CATALYSIS OF SULFONAMIDE HYDROLYSIS BY A NEIGHBOURING CARBOXYL GROUP Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/chin.197503118 |
0.312 |
|
| 1974 |
Aldersley MF, Kirby AJ, Lancaster PW. Intramolecular displacement of alkoxide ions by the ionised carboxy-group: hydrolysis of alkyl hydrogen dialkylmaleates Journal of the Chemical Society-Perkin Transactions 1. 5: 1504-1510. DOI: 10.1039/P29740001504 |
0.48 |
|
| 1974 |
Kirby AJ, McDonald RS, Smith CR. Intramolecular catalysis of amide hydrolysis by two carboxy-groups Journal of the Chemical Society-Perkin Transactions 1. 5: 1495-1504. DOI: 10.1039/P29740001495 |
0.479 |
|
| 1974 |
Aldersley MF, Kirby AJ, Lancaster PW, McDonald RS, Smith CR. Intramolecular catalysis of amide hydrolysis by the carboxy-group. Rate determining proton transfer from external general acids in the hydrolysis of substituted maleamic acids Journal of the Chemical Society-Perkin Transactions 1. 5: 1487-1495. DOI: 10.1039/P29740001487 |
0.482 |
|
| 1974 |
Kirby AJ, Lloyd GJ. Intramolecular general base catalysis of intramolecular nucleophilic catalysis of ester hydrolysis Journal of the Chemical Society-Perkin Transactions 1. 5: 637-642. DOI: 10.1039/P29740000637 |
0.454 |
|
| 1974 |
Craze G, Kirby AJ. The role of the carboxy-group in intramolecular catalysis of acetal hydrolysis. The hydrolysis of substituted 2-methoxymethoxybenzoic acids Journal of the Chemical Society-Perkin Transactions 1. 5: 61-66. DOI: 10.1039/P29740000061 |
0.472 |
|
| 1974 |
Wagenaar A, Kirby A, Engberts JB. Intramolecular catalysis of sulfonamide hydrolysis by a neighbouring carboxyl group Tetrahedron Letters. 15: 3735-3738. DOI: 10.1016/S0040-4039(01)91994-X |
0.425 |
|
| 1974 |
KIRBY AJ, MCDONALD RS, SMITH CR. ChemInform Abstract: INTRAMOLECULAR CATALYSIS OF AMIDE HYDROLYSIS BY TWO CARBOXY-GROUPS Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/chin.197451194 |
0.302 |
|
| 1974 |
ALDERSLEY MF, KIRBY AJ, LANCASTER PW, MCDONALD RS, SMITH CR. ChemInform Abstract: INTRAMOLECULAR CATALYSIS OF AMIDE HYDROLYSIS BY THE CARBOXY-GROUP, RATE DETERMINING PROTON TRANSFER FROM EXTERNAL GENERAL ACIDS IN THE HYDROLYSIS OF SUBSTITUTED MALEAMIC ACIDS Chemischer Informationsdienst. 5. DOI: 10.1002/chin.197451193 |
0.335 |
|
| 1974 |
KIRBY AJ, LLOYD GJ. ChemInform Abstract: INTRAMOLECULAR GENERAL BASE CATALYSIS OF INTRAMOLECULAR NUCLEOPHILIC CATALYSIS OF ESTER HYDROLYSIS Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/chin.197433184 |
0.321 |
|
| 1974 |
KIRBY AJ, LANCASTER PW, SMITH CR. ChemInform Abstract: STRUCTURE AND MECHANISM OF INTRAMOLECULAR CATALYSIS Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/Chin.197432114 |
0.322 |
|
| 1974 |
CRAZE G, KIRBY AJ. ChemInform Abstract: THE ROLE OF THE CARBOXY-GROUP IN INTRAMOLECULAR CATALYSIS OF ACETAL HYDROLYSIS, THE HYDROLYSIS OF SUBSTITUTED 2-METHOXYMETHOXYBENZOIC ACIDS Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/chin.197412123 |
0.34 |
|
| 1972 |
Aldersley MF, Kirby AJ, Lancaster PW. Intramolecular displcement of methoxide by the ionised carboxy-group Journal of the Chemical Society, Chemical Communications. 834-835. DOI: 10.1039/C39720000834 |
0.438 |
|
| 1972 |
Aldersley MF, Kirby AJ, Lancaster PW. Rate-determining proton transfer in intramolecular catalysis of amide hydrolysis by the carboxylic acid group Journal of the Chemical Society, Chemical Communications. 570-571. DOI: 10.1039/C39720000570 |
0.414 |
|
| 1968 |
Fersht AR, Kirby AJ. Intramolecular nucleophilic catalysis in the hydrolysis of substituted aspirin acids. Journal of the American Chemical Society. 90: 5826-32. PMID 5679173 |
0.624 |
|
| 1968 |
Fersht AR, Kirby AJ. Intramolecular nucleophilic catalysis of ester hydrolysis by the ionized carboxyl group. The hydrolysis of 3,5-dinitroaspirin anion. Journal of the American Chemical Society. 90: 5818-26. PMID 5679172 |
0.654 |
|
| 1968 |
Fersht AR, Kirby AJ. Series nucleophilic catalysis in the hydrolysis of 3-acetoxyphthalate. Intramolecular catalysis of ester hydrolysis by the carboxyl group once removed Journal of the American Chemical Society. 90: 5833-5838. DOI: 10.1021/ja01023a030 |
0.361 |
|
| 1967 |
Fersht AR, Kirby AJ. The hydrolysis of aspirin. Intramolecular general base catalysis of ester hydrolysis. Journal of the American Chemical Society. 89: 4857-63. PMID 6074803 DOI: 10.1021/Ja00995A007 |
0.652 |
|
| 1967 |
Fersht AR, Kirby AJ. Structure and mechanism in intramolecular catalysis. The hydrolysis of substituted aspirins. Journal of the American Chemical Society. 89: 4853-6. PMID 6074802 DOI: 10.1021/Ja00995A006 |
0.632 |
|
| 1967 |
Fersht AR, Kirby AJ. Intramolecular general acid catalysis of ester hydrolysis by the carboxylic acid group Journal of the American Chemical Society. 89: 5961-5962. DOI: 10.1021/Ja00999A045 |
0.412 |
|
| 1967 |
Fersht AR, Kirby AJ. Intramolecular nucleophilic catalysis of ester hydrolysis by the carboxylate group Journal of the American Chemical Society. 89: 5960-5961. DOI: 10.1021/Ja00999A044 |
0.451 |
|
| 1967 |
Kirby AJ, Varvoglis AG. The Reactivity of Phosphate Esters. Monoester Hydrolysis Journal of the American Chemical Society. 89: 415-423. DOI: 10.1021/Ja00978A044 |
0.689 |
|
| 1966 |
Kirby AJ, Varvoglis AG. 2,4-Dinitrophenyl Phosphate Journal of the American Chemical Society. 88: 1823-1824. DOI: 10.1021/Ja00960A048 |
0.631 |
|
| 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 |
0.649 |
|
| 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 |
0.596 |
|
| Show low-probability matches. |