| Year |
Citation |
Score |
| 2020 |
Greaves ME, Ronson TO, Lloyd-Jones GC, Maseras F, Sproules S, Nelson DJ. Unexpected Nickel Complex Speciation Unlocks Alternative Pathways for the Reactions of Alkyl Halides with dppf-Nickel(0). Acs Catalysis. 10: 10717-10725. PMID 32983589 DOI: 10.1021/Acscatal.0C02514 |
0.563 |
|
| 2019 |
Bauer M, Cadge J, Davies D, Durand DJ, Eisenstein O, Ess D, Fey N, Gallarati S, George M, Hamilton A, Harvey J, Hintermair U, Hulme AN, Ishii Y, Jensen VR, ... Lloyd-Jones G, et al. Computational and theoretical approaches for mechanistic understanding: general discussion. Faraday Discussions. PMID 31764927 DOI: 10.1039/C9Fd90073J |
0.744 |
|
| 2019 |
Aoki Y, Bauer M, Braun T, Cadge J, Davies D, Durand DJ, Eisenstein O, Ess D, Fairlamb I, Fey N, Gallarati S, George M, Greaves M, Halse M, Hamilton A, ... ... Lloyd-Jones G, et al. Physical methods for mechanistic understanding: general discussion. Faraday Discussions. PMID 31755887 DOI: 10.1039/C9Fd90070E |
0.732 |
|
| 2019 |
Aoki Y, Braun T, Davies D, Eisenstein O, Fairlamb I, Fey N, George M, Goult C, Hamilton A, Huang Z, Ishii Y, Jakoobi M, Kuwata S, Lloyd-Jones G, Love J, et al. Understanding unusual element-element bond formation and activation: general discussion. Faraday Discussions. PMID 31755882 DOI: 10.1039/C9Fd90071C |
0.742 |
|
| 2019 |
Aoki Y, Bauer M, Braun T, Cadge JA, Clarke GE, Durand DJ, Eisenstein O, Gallarati S, Greaves M, Harvey J, Haynes A, Hintermair U, Hulme AN, Ishii Y, Jakoobi M, ... ... Lloyd-Jones G, et al. Mechanistic insight into organic and industrial transformations: general discussion. Faraday Discussions. PMID 31754665 DOI: 10.1039/C9Fd90072A |
0.561 |
|
| 2018 |
Johnston C, West T, Dooley R, Reid M, Jones AB, King E, Leach AG, Lloyd-Jones GC. Anion-Initiated Trifluoromethylation by TMSCF3: Deconvolution of the Siliconate-Carbanion Dichotomy by Stopped-Flow NMR/IR. Journal of the American Chemical Society. PMID 30080973 DOI: 10.1021/Jacs.8B06777 |
0.682 |
|
| 2018 |
Keske EC, West TH, Lloyd-Jones GC. Analysis of Autoinduction, Inhibition, and Autoinhibition in a Rh-Catalyzed C–C Cleavage: Mechanism of Decyanative Aryl Silylation Acs Catalysis. 8: 8932-8940. DOI: 10.1021/acscatal.8b02809 |
0.747 |
|
| 2017 |
Cox PA, Reid M, Leach AG, Campbell AD, King EJ, Lloyd-Jones GC. Base-catalyzed Aryl-B(OH)2 Protodeboronation Revisited: from Concerted Proton-Transfer to Liberation of a Transient Arylanion. Journal of the American Chemical Society. PMID 28823150 DOI: 10.1021/Jacs.7B07444 |
0.67 |
|
| 2016 |
Corrie TJ, Ball LT, Russell CA, Lloyd-Jones GC. Au-catalyzed Biaryl Coupling to Generate 5- to 9-membered Rings: Turnover-Limiting Reductive Elimination versus π-complexation. Journal of the American Chemical Society. PMID 27936749 DOI: 10.1021/Jacs.6B10018 |
0.745 |
|
| 2016 |
Lloyd-Jones GC, Cresswell A. Room Temperature Gold-Catalysed Arylation of Heteroarenes: Complementarity to Palladium Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27325239 DOI: 10.1002/Chem.201602893 |
0.728 |
|
| 2015 |
Racys DT, Eastoe J, Norrby PO, Grillo I, Rogers SE, Lloyd-Jones GC. Pd- η(3) -C6H9 complexes of the Trost modular ligand: high nuclearity columnar aggregation controlled by concentration, solvent and counterion. Chemical Science. 6: 5793-5801. PMID 28791087 DOI: 10.1039/C5Sc01181G |
0.533 |
|
| 2015 |
Murray AT, Dowley MJ, Pradaux-Caggiano F, Baldansuren A, Fielding AJ, Tuna F, Hendon CH, Walsh A, Lloyd-Jones GC, John MP, Carbery DR. Catalytic Amine Oxidation under Ambient Aerobic Conditions: Mimicry of Monoamine Oxidase B. Angewandte Chemie (International Ed. in English). 54: 8997-9000. PMID 26087676 DOI: 10.1002/Anie.201503654 |
0.325 |
|
| 2015 |
Lennox A, Lloyd-Jones G. Boron reagent activation in Suzuki-Miyaura coupling Rsc Catalysis Series. 2015: 322-354. |
0.748 |
|
| 2014 |
Lloyd-Jones GC, Ball LT. Catalysis. Self-control tames the coupling of reactive radicals. Science (New York, N.Y.). 345: 381-2. PMID 25061190 DOI: 10.1126/Science.1256755 |
0.707 |
|
| 2014 |
Ball LT, Lloyd-Jones GC, Russell CA. Gold-catalyzed oxidative coupling of arylsilanes and arenes: origin of selectivity and improved precatalyst. Journal of the American Chemical Society. 136: 254-64. PMID 24367895 DOI: 10.1021/Ja408712E |
0.758 |
|
| 2014 |
Lennox AJ, Lloyd-Jones GC. Selection of boron reagents for Suzuki-Miyaura coupling. Chemical Society Reviews. 43: 412-43. PMID 24091429 DOI: 10.1039/C3Cs60197H |
0.767 |
|
| 2012 |
Jover J, Fey N, Harvey JN, Lloyd-Jones GC, Orpen AG, Owen-Smith GJ, Murray P, Hose DR, Osborne R, Purdie M. Expansion of the Ligand Knowledge Base for Chelating P,P-Donor Ligands (LKB-PP). Organometallics. 31: 5302-5306. PMID 24882917 DOI: 10.1021/Om300312T |
0.756 |
|
| 2012 |
Ball LT, Lloyd-Jones GC, Russell CA. Gold-catalyzed direct arylation. Science (New York, N.Y.). 337: 1644-8. PMID 23019647 DOI: 10.1126/Science.1225709 |
0.742 |
|
| 2012 |
Ball LT, Lloyd-Jones GC, Russell CA. Gold-catalysed oxyarylation of styrenes and mono- and gem-disubstituted olefins facilitated by an iodine(III) oxidant. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 2931-7. PMID 22298471 DOI: 10.1002/Chem.201103061 |
0.758 |
|
| 2011 |
Tan EH, Lloyd-Jones GC, Harvey JN, Lennox AJ, Mills BM. [(RCN)2PdCl2]-catalyzed E/Z isomerization of alkenes: a non-hydride binuclear addition-elimination pathway. Angewandte Chemie (International Ed. in English). 50: 9602-6. PMID 21938759 DOI: 10.1002/Anie.201103947 |
0.765 |
|
| 2011 |
Stará IG, Andronova A, Kollárovič A, Vyskočil S, Jugé S, Lloyd-Jones GC, Guiry PJ, Starý I. Enantioselective [2+2+2] cycloisomerisation of alkynes in the synthesis of helicenes: The search for effective chiral ligands Collection of Czechoslovak Chemical Communications. 76: 2005-2022. DOI: 10.1135/Cccc2011177 |
0.586 |
|
| 2011 |
Tan EHP, Lloyd-Jones GC, Harvey JN, Lennox AJJ, Mills BM. [(RCN) 2PdCl 2]-catalyzed E/Z isomerization of alkenes: A non-hydride binuclear addition-elimination pathway Angewandte Chemie - International Edition. 50: 9602-9606. DOI: 10.1002/anie.201103947 |
0.466 |
|
| 2010 |
Ball LT, Green M, Lloyd-Jones GC, Russell CA. Arylsilanes: application to gold-catalyzed oxyarylation of alkenes. Organic Letters. 12: 4724-7. PMID 20879724 DOI: 10.1021/Ol1019162 |
0.762 |
|
| 2010 |
Butters M, Harvey JN, Jover J, Lennox AJ, Lloyd-Jones GC, Murray PM. Aryl trifluoroborates in Suzuki-Miyaura coupling: the roles of endogenous aryl boronic acid and fluoride. Angewandte Chemie (International Ed. in English). 49: 5156-60. PMID 20544767 DOI: 10.1002/Anie.201001522 |
0.759 |
|
| 2010 |
Alder RW, Harvey JN, Lloyd-Jones GC, Oliva JM. Can (pi)6 + (pi)4 = 10? Exploring cycloaddition routes to highly unsaturated 10-membered rings. Journal of the American Chemical Society. 132: 8325-37. PMID 20509653 DOI: 10.1021/Ja1008135 |
0.468 |
|
| 2010 |
Sloan ME, Staubitz A, Clark TJ, Russell CA, Lloyd-Jones GC, Manners I. Homogeneous catalytic dehydrocoupling/dehydrogenation of amine-borane adducts by early transition metal, group 4 metallocene complexes. Journal of the American Chemical Society. 132: 3831-41. PMID 20180565 DOI: 10.1021/Ja909535A |
0.452 |
|
| 2010 |
Eastoe J, Fairlamb IJS, Fernández-Hernández JM, Filali E, Jeffery JC, Lloyd-Jones GC, Martorell A, Meadowcroft A, Norrby PO, Riis-Johannessen T, Sale DA, Tomlin PM. Interrogation of a dynamic multi-catalyst ensemble in asymmetric catalysis Faraday Discussions. 145: 27-47. DOI: 10.1039/B910022A |
0.548 |
|
| 2010 |
Jover J, Fey N, Harvey JN, Lloyd-Jones GC, Orpen AG, Owen-Smith GJJ, Murray P, Hose DRJ, Osborne R, Purdie M. Expansion of the ligand knowledge base for monodentate P-donor ligands (LKB-P) Organometallics. 29: 6245-6258. DOI: 10.1021/Om100648V |
0.761 |
|
| 2010 |
Alder RW, Harvey JN, Lloyd-Jones GC, Oliva JM. Can π6+π4 = 10- Exploring cycloaddition routes to highly unsaturated 10-membered rings Journal of the American Chemical Society. 132: 8325-8337. DOI: 10.1021/ja1008135 |
0.44 |
|
| 2010 |
Johansson C, Lloyd-Jones GC, Norrby PO. Memory and dynamics in Pd-catalyzed allylic alkylation with P,N-ligands Tetrahedron Asymmetry. 21: 1585-1592. DOI: 10.1016/J.Tetasy.2010.03.031 |
0.529 |
|
| 2010 |
Norrby PO, Lloyd-Jones GC. Journal of Molecular Catalysis A: Chemical: Editorial Journal of Molecular Catalysis a: Chemical. 324: 1-2. DOI: 10.1016/j.molcata.2010.04.001 |
0.418 |
|
| 2010 |
Jover J, Fey N, Purdie M, Lloyd-Jones GC, Harvey JN. A computational study of phosphine ligand effects in Suzuki-Miyaura coupling Journal of Molecular Catalysis a: Chemical. 324: 39-47. DOI: 10.1016/J.Molcata.2010.02.021 |
0.789 |
|
| 2010 |
Koch G, Lloyd-Jones GC, Loiseleur O, Pfaltz A, Prétôt R, Schaffner S, Schnider P, von Matt P. Synthesis of chiral (phosphinoaryl)oxazolines, a versatile class of ligands for asymmetric catalysis Recueil Des Travaux Chimiques Des Pays-Bas. 114: 206-210. DOI: 10.1002/recl.19951140413 |
0.509 |
|
| 2010 |
LEHMANN J, LLOYD-JONES GC. ChemInform Abstract: Regiocontrol and Stereoselectivity in Tungsten-Bipyridine Catalyzed Allylic Alkylation. Cheminform. 26: no-no. DOI: 10.1002/chin.199548079 |
0.307 |
|
| 2010 |
KOCH G, LLOYD-JONES GC, LOISELEUR O, PFALTZ A, PRETOT R, SCHAFFNER S, SCHNIDER P, VON MATT P. ChemInform Abstract: Synthesis of Chiral (Phosphinoaryl)oxazolines, a Versatile Class of Ligands for Asymmetric Catalysis. Cheminform. 26: no-no. DOI: 10.1002/chin.199542182 |
0.513 |
|
| 2010 |
VON MATT P, LLOYD-JONES GC, MINIDIS ABE, PFALTZ A, MACKO L, NEUBURGER M, ZEHNDER M, RUEEGGER H, PREGOSIN PS. ChemInform Abstract: Enantioselective Allylic Substitution Catalyzed by Chiral Bis( dihydrooxazole)palladium Complexes: Catalyst Structure and Possible Mechanism of Enantioselection. Cheminform. 26: no-no. DOI: 10.1002/chin.199531108 |
0.526 |
|
| 2010 |
LLOYD-JONES GC, PFALTZ A. ChemInform Abstract: Chiral Phosphanodihydrooxazoles in Asymmetric Catalysis: Tungsten- Catalyzed Allylic Substitution. Cheminform. 26: no-no. DOI: 10.1002/chin.199528070 |
0.522 |
|
| 2010 |
BROWN JM, LLOYD-JONES GC. ChemInform Abstract: Vinylborane Formation in Rhodium-Catalyzed Hydroborations. Ligand-Free Homogeneous Catalysis. Cheminform. 23: no-no. DOI: 10.1002/chin.199239237 |
0.317 |
|
| 2009 |
Harvey JN, Jover J, Lloyd-Jones GC, Moseley JD, Murray P, Renny JS. The Newman-Kwart rearrangement of O-aryl thiocarbamates: substantial reduction in reaction temperatures through palladium catalysis. Angewandte Chemie (International Ed. in English). 48: 7612-5. PMID 19746383 DOI: 10.1002/Anie.200903908 |
0.772 |
|
| 2009 |
Evans LA, Fey N, Lloyd-Jones GC, Muñoz MP, Slatford PA. Cryptocatalytic 1,2-alkene migration in a σ-alkyl palladium diene complex Angewandte Chemie - International Edition. 48: 6262-6265. PMID 19618412 DOI: 10.1002/Anie.200901468 |
0.726 |
|
| 2009 |
Butts CP, Filali E, Lloyd-Jones GC, Norrby PO, Sale DA, Schramm Y. Structure-based rationale for selectivity in the asymmetric allylic alkylation of cycloalkenyl esters employing the Trost 'Standard Ligand' (TSL): isolation, analysis and alkylation of the monomeric form of the cationic eta(3)-cyclohexenyl complex [(eta(3)-c-C6H9)Pd(TSL)]+. Journal of the American Chemical Society. 131: 9945-57. PMID 19435358 DOI: 10.1021/Ja8099757 |
0.539 |
|
| 2009 |
Lloyd-Jones G, Evans L, Fey N, Harvey J, Hose D, Murray P, Orpen A, Osborne R, Owen-Smith G, Purdie M. Kinetic Studies of Palladium-Catalyzed Tsuji-Trost Allylations Synfacts. 2009: 0292-0292. DOI: 10.1055/S-0028-1087759 |
0.795 |
|
| 2008 |
Evans LA, Fey N, Harvey JN, Hose D, Lloyd-Jones GC, Murray P, Orpen AG, Osborne R, Owen-Smith GJJ, Purdie M. Counterintuitive kinetics in Tsuji-Trost allylation: Ion-pair partitioning and implications for asymmetric catalysis Journal of the American Chemical Society. 130: 14471-14473. PMID 18839958 DOI: 10.1021/Ja806278E |
0.781 |
|
| 2008 |
Dyke AM, Gill DM, Harvey JN, Hester AJ, Lloyd-Jones GC, Muñoz MP, Shepperson IR. Decoupling deprotonation from metalation: Thia-fries rearrangement Angewandte Chemie - International Edition. 47: 5067-5070. PMID 18504791 DOI: 10.1002/Anie.200800750 |
0.43 |
|
| 2008 |
Fey N, Harvey JN, Lloyd-Jones GC, Murray P, Orpen AG, Osborne R, Purdie M. Computational descriptors for chelating P,P- And P,N-donor ligands Organometallics. 27: 1372-1383. DOI: 10.1021/Om700840H |
0.783 |
|
| 2008 |
Barta K, Franciò G, Leitner W, Lloyd-Jones GC, Shepperson IR. A new class of 3′-sulfonyl binaphos ligands: Modulation of activity and selectivity in asymmetric palladium-catalysed hydrophosphorylation of styrene Advanced Synthesis and Catalysis. 350: 2013-2023. DOI: 10.1002/Adsc.200800366 |
0.482 |
|
| 2006 |
Bray KL, Lloyd-Jones GC, Muñoz MP, Slatford PA, Tan EHP, Tyler-Mahon AR, Worthington PA. Mechanism of cycloisomerisation of 1,6-heptadienes catalysed by [(tBuCN)2PdCl2]: Remarkable influence of exogenous and endogenous 1,6- And 1,5-diene ligands Chemistry - a European Journal. 12: 8650-8663. PMID 17048286 DOI: 10.1002/chem.200600924 |
0.322 |
|
| 2006 |
Malkov AV, Gouriou L, Lloyd-Jones GC, Starý I, Langer V, Spoor P, Vinader V, Kočovský P. Asymmetric allylic substitution catalyzed by C1-symmetrical complexes of molybdenum: Structural requirements of the ligand and the stereochemical course of the reaction Chemistry - a European Journal. 12: 6910-6929. PMID 16807930 DOI: 10.1002/chem.200501574 |
0.312 |
|
| 2006 |
Luft JAR, Yu ZX, Hughes DL, Lloyd-Jones GC, Krska SW, Houk KN. On the stability of the π-allyl intermediate in molybdenum-catalyzed asymmetric alkylations Tetrahedron Asymmetry. 17: 716-724. DOI: 10.1016/J.Tetasy.2006.01.037 |
0.631 |
|
| 2004 |
Hughes DL, Lloyd-Jones GC, Krska SW, Gouriou L, Bonnet VD, Jack K, Sun Y, Mathre DJ, Reamer RA. Mechanistic studies of the molybdenum-catalyzed asymmetric alkylation reaction. Proceedings of the National Academy of Sciences of the United States of America. 101: 5379-84. PMID 15056759 DOI: 10.1073/Pnas.0306918101 |
0.64 |
|
| 2004 |
Lloyd-Jones GC, Krska SW, Hughes DL, Gouriou L, Bonnet VD, Jack K, Sun Y, Reamer RA. Conclusive evidence for a retention-retention pathway for the molybdenum-catalyzed asymmetric alkylation. Journal of the American Chemical Society. 126: 702-3. PMID 14733529 DOI: 10.1021/Ja0376339 |
0.624 |
|
| 2004 |
Lloyd-Jones GC, Stephen SC, Fairlamb IJS, Martorell A, Dominguez B, Tomlin PM, Murray M, Fernandez JM, Jeffery JC, Riis-Johannessen T, Guerziz T. Coordination of the Trost modular ligand to palladium allyl fragments: Oligomers, monomers and memory effects in catalysis Pure and Applied Chemistry. 76: 589-601. DOI: 10.1351/Pac200476030589 |
0.349 |
|
| 2004 |
Fairlamb IJS, Lloyd-Jones GC, Martorell A, Murray M, Stephen SC, Tomlin PM. ISOTOPIC DESYMMETRIZATION IN THE STUDY OF HOMOGENEOUS CATALYSIS Phosphorus, Sulfur, and Silicon and the Related Elements. 179: 907-910. DOI: 10.1080/10426500490428889 |
0.319 |
|
| 2003 |
Lloyd-Jones GC, Harvey JN, Hodgson P, Murray M, Woodward RL. Scalar coupling between the 15N centres in methylated 1,8-diaminonaphthalenes and 1,6-diazacyclodecane: to what extent is 2HJNN a reliable indicator of N-N distance? Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 4523-35. PMID 14502638 DOI: 10.1002/Chem.200304890 |
0.43 |
|
| 2002 |
Fairlamb IJ, Lloyd-Jones GC, Vyskocil S, Kocovský P. Analysis of stereochemical convergence in asymmetric pd-catalysed allylic alkylation reactions complicated by halide and memory effects. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 4443-53. PMID 12355532 DOI: 10.1002/1521-3765(20021004)8:19<4443::Aid-Chem4443>3.0.Co;2-3 |
0.643 |
|
| 2001 |
Bray KL, Charmant JP, Fairlamb IJ, Lloyd-Jones GC. Structural and mechanistic studies on the activation and propagation of a cationic allylpalladium procatalyst in 1,6-diene cycloisomerization. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 4205-15. PMID 11686600 DOI: 10.1002/1521-3765(20011001)7:19<4205::Aid-Chem4205>3.0.Co;2-Q |
0.59 |
|
| 1998 |
Prétôt R, Lloyd-Jones GC, Pfaltz A. Enantio- and regiocontrol in palladium- and tungsten-catalyzed allylic substitutions Pure and Applied Chemistry. 70: 1035-1040. DOI: 10.1351/Pac199870051035 |
0.618 |
|
| 1995 |
Matt PV, Lloyd-Jones GC, Minidis ABE, Pfaltz A, Macko L, Neuburger M, Zehnder M, Rüegger H, Pregosin PS. Enantioselective Allylic Substitution Catalyzed by Chiral [Bis(dihydrooxazole)]palladium Complexes: Catalyst structure and possible mechanism of enantioselection Helvetica Chimica Acta. 78: 265-284. DOI: 10.1002/Hlca.19950780202 |
0.572 |
|
| 1995 |
Lloyd-Jones GC, Pfaltz A. Chiral Phosphanodihydrooxazoles in Asymmetric Catalysis: Tungsten-Catalyzed Allylic Substitution Angewandte Chemie International Edition in English. 34: 462-464. DOI: 10.1002/anie.199504621 |
0.524 |
|
| 1995 |
Lloyd-Jones GC, Pfaltz A. Chirale Phosphanodihydrooxazole in der asymmetrischen Katalyse: Wolfram-katalysierte allylische Substitution Angewandte Chemie. 107: 534-536. DOI: 10.1002/Ange.19951070430 |
0.459 |
|
| 1994 |
Brown JM, Lloyd-Jones GC. Vinylborane Formation in Rhodium-Catalyzed Hydroboration of Vinylarenes. Mechanism versus Borane Structure and Relationship to Silation Journal of the American Chemical Society. 116: 866-878. DOI: 10.1021/Ja00082A006 |
0.436 |
|
| 1993 |
Brown JM, Lloyd-Jones GC, Layzell TP. Reversible dimerisation of ephedrine-derived oxazaborolidines Tetrahedron: Asymmetry. 4: 2151-2154. DOI: 10.1016/S0957-4166(00)80063-4 |
0.313 |
|
| 1992 |
Brown JM, Leppard SW, Lloyd-Jones GC. A rapid assay for the enantiomeric purity of secondary alcohols using 4S,5R-4-methyl,5-phenyl-1,3,2-oxazaborolidine (ephedrineborane). Tetrahedron: Asymmetry. 3: 261-266. DOI: 10.1016/S0957-4166(00)80205-0 |
0.348 |
|
| 1990 |
Brown JM, Lloyd-Jones GC. Catalytic asymmetric hydroboration with oxazaborolidines Tetrahedron: Asymmetry. 1: 869-872. DOI: 10.1016/S0957-4166(00)82276-4 |
0.416 |
|
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