Chemoselective oxidation of aryl organoboron systems enabled by boronic acid-selective phase transferThe Newman-Kwart rearrangement of O-aryl thiocarbamates: substantial reduction in reaction temperatures through palladium catalysis.Aryl trifluoroborates in Suzuki-Miyaura coupling: the roles of endogenous aryl boronic acid and fluoride.Gold-catalyzed direct arylation.Mechanistic studies of the molybdenum-catalyzed asymmetric alkylation reaction.Diverse and potentially manipulative signalling with ascarosides in the model nematode C. elegansCatalytic Amine Oxidation under Ambient Aerobic Conditions: Mimicry of Monoamine Oxidase BMIDA boronates are hydrolysed fast and slow by two different mechanisms.Catalytic Enantioselective [2,3]-Rearrangements of Allylic Ammonium Ylides: A Mechanistic and Computational Study.Transmetalation in the Suzuki-Miyaura coupling: the fork in the trail.Selection of boron reagents for Suzuki-Miyaura coupling.Au-Catalyzed Biaryl Coupling To Generate 5- to 9-Membered Rings: Turnover-Limiting Reductive Elimination versus π-Complexation.Use of reactive tracers to determine ambient OH radical concentrations: application within the indoor environment.Expansion of the Ligand Knowledge Base for Chelating P,P-Donor Ligands (LKB-PP).Pd- η3 -C6H9 complexes of the Trost modular ligand: high nuclearity columnar aggregation controlled by concentration, solvent and counterion.Mechanism of phosphine borane deprotection with amines: the effects of phosphine, solvent and amine on rate and efficiency.Hindered ureas as masked isocyanates: facile carbamoylation of nucleophiles under neutral conditions.Room-temperature palladium-catalyzed C-H activation: ortho-carbonylation of aniline derivatives.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 [Readily accessible, modular, and tuneable BINOL 3,3'-perfluoroalkylsulfones: highly efficient catalysts for enantioselective in-mediated imine allylation.Chiral perylene diimides: building blocks for ionic self-assemblyThe molecularity of the Newman-Kwart rearrangement.Facile double-lithiation of a transient urea: vicarious ortho-metalation of aniline derivatives.Can (pi)6 + (pi)4 = 10? Exploring cycloaddition routes to highly unsaturated 10-membered rings.Distinct reactivity of Pd(OTs)2: the intermolecular Pd(II)-catalyzed 1,2-carboamination of dienes.Homogeneous catalytic dehydrocoupling/dehydrogenation of amine-borane adducts by early transition metal, group 4 metallocene complexes.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?Mechanisms of the thermal and catalytic redistributions, oligomerizations, and polymerizations of linear diborazanes.Gold-catalyzed oxidative coupling of arylsilanes and arenes: origin of selectivity and improved precatalyst.Conclusive evidence for a retention-retention pathway for the molybdenum-catalyzed asymmetric alkylation.Unusually Large Primary (2)H/(1)H Kinetic Isotope Effects Accompanying a syn-beta-H Elimination Reaction in a sigma-Alkyl-Palladium Complex.On the preparation of ortho-trifluoromethyl phenyl triflate.Dehydrocoupling of dimethylamine borane catalyzed by Rh(PCy3)2H2Cl.Counterintuitive kinetics in Tsuji-Trost allylation: ion-pair partitioning and implications for asymmetric catalysis.BINOL-3,3'-triflone N,N-dimethyl phosphoramidites: through-space 19F,31P spin-spin coupling with a remarkable dependency on temperature and solvent internal pressure.Pd(II)-catalyzed intermolecular 1,2-diamination of conjugated dienes.Protodeboronation of Heteroaromatic, Vinyl, and Cyclopropyl Boronic Acids: pH-Rate Profiles, Autocatalysis, and Disproportionation.Decoupling deprotonation from metalation: Thia-Fries rearrangement.Mechanistic studies of the dehydrocoupling and dehydropolymerization of amine-boranes using a [Rh(Xantphos)]⁺ catalyst.Gold-Triggered Uncaging Chemistry in Living Systems.
P50
Q33749691-E16BEFD7-1A2F-4075-81D7-F43BDBAD0B7CQ34019345-CBEC7F5B-F1EF-443A-BDF9-12F5716928DAQ34120623-7C5FEA7F-9CEA-4EEE-8C09-F8902FAE7E3BQ34302458-AC14955C-71C2-47D7-AD81-C02433EFF6E4Q34310124-06413A51-DA28-40E2-850A-FC3E05F7152EQ35117427-A0217F5A-32FB-4979-9BF5-BE41D0EF33C6Q35914850-324FA4D5-852A-4636-8FEB-5EA0B7E23778Q37422908-F26C96D6-DA28-4D69-89C4-F228C0E1C754Q37731437-F16F5DB1-2233-49B9-AFB4-E3EE7BF9703CQ38115488-65A24A3C-28B8-41DA-ADA1-D8D107BC11F1Q38148935-7AA7E054-9B94-486D-9066-EC0EA55EC2C5Q39114416-ACBBE22F-1779-45EE-B035-B1C4415B3CEEQ39848238-F02D70F8-9A66-48EC-A526-068D60BF560BQ39949844-4FE8A7BC-E8FC-4F30-B48C-39740764D2F0Q41083107-9050F52D-1BED-4E48-B9E3-516A8D81C09FQ41372165-4E179BFA-A08B-4A8C-B815-CA2D3DF43E54Q41893105-B4920C29-FFB6-4C07-85F0-A3082DA5D388Q41951011-370D4D73-7D0D-4E22-9A66-D1833CEE35D4Q42163089-053F9ED0-6CAD-40E2-A81D-80BF1673DE95Q42163604-CE4C744F-8FBC-49F4-80CE-C1B60264FEA0Q42380966-E6ED9645-D9A6-411A-88B0-2828CC48711DQ42919466-E1A71D49-D2C1-49D6-B083-1C1083767B93Q43043072-46A1DFA6-F39F-4274-BD6D-C6F0938F2659Q43051477-4B5B1403-D35E-42C5-A473-40DC5A6C64FEQ43139123-B7D20A7E-943B-4359-A192-43A16E655371Q43151827-37E86416-33F4-41C1-B59D-7F7F60EA2601Q44591928-1EF2038F-139D-45E5-960D-E4F44D4C66B9Q44643539-BBA4F863-DF25-412A-BCF1-90FA26C42AB6Q44665778-EC71BF2D-A9F8-44A3-B025-73712740E893Q44735033-61577B61-5084-4662-ABC4-890C73177FEDQ44783166-A1E32F39-2BF6-4B76-A208-A6E5551204F4Q45028328-C6BBF5E7-A620-46DE-B595-B9BDD9C97D53Q45710932-2C9F5062-9C81-4866-BF5D-519238D0D3CBQ46327984-6AD8FCBE-33B1-4C4D-8961-04E951DA940EQ46472391-0541A6D8-C92B-4542-8C34-870EDE44D5E9Q46494660-1316E0B4-9690-4D18-B26C-15588A90DCD0Q46525722-FF577412-E981-4E47-9FC3-2C658A739AE8Q46574277-9ADB85DA-DE76-4040-AE02-90FF92C099C4Q46892296-787E80A5-3C5B-455B-9D58-DBB4EA663F18Q47111183-857DBDBE-018D-4849-A11A-0F89656E1F2C
P50
description
British academic
@en
British academic
@en-ca
British academic
@en-gb
académico británico
@es
scheikundige
@nl
أكاديمي بريطاني
@ar
name
Guy Lloyd-Jones
@ast
Guy Lloyd-Jones
@en
Guy Lloyd-Jones
@es
Guy Lloyd-Jones
@fr
Guy Lloyd-Jones
@nl
Guy Lloyd-Jones
@sl
type
label
Guy Lloyd-Jones
@ast
Guy Lloyd-Jones
@en
Guy Lloyd-Jones
@es
Guy Lloyd-Jones
@fr
Guy Lloyd-Jones
@nl
Guy Lloyd-Jones
@sl
prefLabel
Guy Lloyd-Jones
@ast
Guy Lloyd-Jones
@en
Guy Lloyd-Jones
@es
Guy Lloyd-Jones
@fr
Guy Lloyd-Jones
@nl
Guy Lloyd-Jones
@sl
P166
P101
P106
P1153
7005241494
P19
P2070
guy-lloyd-jones-11829
P21
P2381
P31
P463
P496
0000-0003-2128-6864
P569
1966-05-17T00:00:00Z