LENNOX LAB

[28] Alkene Vicinal Difluorination: From Fluorine gas to more Favoured conditions

S. Doobary and A. J. J. Lennox*

Synlett, 2020, DOI: 10.1055/s-0040-1707143

[27] Electrode Materials in Modern Organic Electrochemistry

D. M. Heard and A. J. J. Lennox*,

Angew. Chem. Int. Ed. 2020, DOI: 10.1002/anie.202005745

[26] Synthesis, Stability and Biological Studies of Fluorinated Analogues of Thromboxane A2

C. Jing, S. Mallah, E. Kriemen, S. H. Bennett, V. Fasano, I. Hers,*
A. J. J. Lennox,* and V. K. Aggarwal*

ACS Central Science, 2020, 6, 995-1000

[25] Minimal Manual Input

D. M. Heard & A. J. J. Lennox*

Nature Chemistry, 2020, 12, 113-114

[24] Electrochemical Vicinal Difluorination of Alkenes: Scalable and Amenable to Electron‐rich Substrates

S. Doobary, A. T. Sedikides, H. P. Caldora, D. L. Poole, A. J. J. Lennox*

Angew. Chem. Int. Ed., 2020, 59, 1155-1160

[23] Meisenheimer Complexes in SNAr Reactions: Intermediates or Transition States?

A. J. J. Lennox*

Angew. Chem. Int. Ed., 2018, 57, 14686–14688

[22] Structural Design of Conjugated Poly (ferrocene-phenanthroline) for Photocatalytic Hydrogen Evolution from Water

Z.-J. Yu, H. Chen, A. J. J. Lennox, L.-J. Yan, X.-F. Liu, D.-D. Xu, F. Chen, L.-X. Xu, Y. Li, Q.-A. Wu, S.-P. Luo,

Dye. Pigment., 2019, 162, 771–775

[21] Electrochemical Aminoxyl-Mediated α-Cyanation of Secondary Piperidines for Pharmaceutical Building Block Diversification

A. J. J. Lennox, S. L. Goes, M. P. Webster, H. F. Koolman, S. W. Djuric, S. S. Stahl*

J. Am. Chem. Soc. 2018, 140, 11227–11231

[20] Structural Design of the Conjugated Poly(ferrocene-phenantholine) for Photocatalytic Hydrogen Evolution from Water

S.-P. Luo,* X.-J. Wang, H. Chen, Z.-J. Yu, W.-Y. Lou, X.-F. Liu, L.-M. Xia, B.-Y. Lou, P. Kang, A. J. J. Lennox, Q.-A. Wu

ChemPhotoChem, 2018, 2, 791–795

[19] Selective electrochemical generation of benzylic radicals enabled by ferrocene-based electron-transfer mediators

A. J. J. Lennox,* J. E. Nutting, S. S. Stahl*

Chem. Sci. 2018, 9, 356-361

[18] Structure activated copper photosensitizers for photocatalytic water reduction

A. J. J. Lennox,#  N.-Y. Chen,#  L.-M. Xia,# Y.-Y. Sun, H. Chen, H.-M. Jin, H. Junge, Q.-A. Wu, J.-H. Jia, M. Beller, S.-P. Luo*

Chem. Eur. J. 2017, 23, 3631-3636,   #equal contribution

[17] H2 generation with (mixed) plasmonic Cu,Ag,Au-TiO2 photocatalysts: Structure-reactivity relationships assessed by in situ spectroscopy

J. B. Priebe, J. Radnik, C. Kreyenschulte, A. J. J. Lennox, H. Junge, M. Beller, A. Brückner*

ChemCatChem, 2017, 9, 1025-1031

[16] Unravelling the Mechanism of basic aqueous Methanol Dehydrogenation catalyzed by Ru-PNP Pincer Complexes

A. J. J. Lennox,# E. Alberico,# L. K. Neumann, H. Jiao, W. Baumann, H.-J. Drexler, M. Nielson, A. Spannenberg, M. P. Checinski, H. Junge, M. Beller*

J. Am. Chem. Soc. 2016, 138, 14890-14908       #equal contribution

[15] Efficient Photocatalytic Water Reduction Using in Situ Generated Knölker's Iron Complexes

Y.-Y. Sun, H. Wang, N.-Y. Chen, A. J. J. Lennox, A. Friedrich, L.-M. Xia, S. Lochbrunner, H. Junge, M. Beller, S. Shou S.-P. Luo*

ChemCatChem, 2016, 8, 2340-2344

[14] In situ Photodeposition of Copper Nanoparticles on TiO2: Novel Catalysts with Facile Light-Induced Redox Cycling

A. J. J. Lennox, P. Bartels, M. M. Pohl, H. Junge, M. Beller*

J. Catal. 2016, 340, 177-183

[13] Copper-Based Photosensitisers in Water Reduction: A More Efficient In Situ Formed System and Improved Mechanistic Understanding

A. J. J. Lennox, S. Fischer, M. Jurrat, S.-P. Lou, N. Rockstroh, H. Junge, R. Ludwig, M. Beller*

Chem. Eur. J., 2016, 22, 1233-1238

[12] Rhodium-catalyzed alkoxylation/ acetalization of diazo compounds: One-step synthesis of highly functionalized quaternary carbon centers

J. Pospech, A. J. J. Lennox, M. Beller*

Chem Commun., 2015, 51, 14505-14508

[11] Solar Hydrogen Production by plasmonic Au-TiO2 catalysts: Impact of Synthesis Protocol and TiO2 Phase on charge transfer efficiency and H2 evolution rates

J. B. Priebe, J. Radnik, A. J. J. Lennox, M.-M. Pohl, M. Karnahl, D. Hollmann, H.Junge, M. Beller, A. Brückner*

ACS Catal., 2015, 5, 2137-2148

[10] A mild and selective reduction of β-Lactams: Rh-catalyzed hydrosilylation towards important pharmacological building blocks

C. Bornschein, A. J. J. Lennox, S. Werkmeister, K. Junge, M. Beller*

Eur. J. Org. Chem., 2015, 2015, 1915-1919

[9] Adding value to Power-Station Captured CO2: Highly tolerant Di-Zn and Mg homogeneous catalysts for polycarbonate polyol production

A. M. Chapman, C. Keyworth, M. R. Kember, A. J. J. Lennox, C. K. Williams*

ACS Catal., 2015, 5, 1581-1588

[8] Boron Reagent Activation in Suzuki-Miyaura Coupling

A. J. J. Lennox, G. C. Lloyd-Jones*

Modern Cross Coupling: Evolution and Application, Ed. Thomas Colacot, RSC Publishing, 2014

[7] Selection of Boron Reagents in Suzuki-Miyaura Coupling

A. J. J. Lennox, G. C. Lloyd-Jones*

Chem. Soc. Rev., 2014, 43, 412-443

[6] Transmetalation in Suzuki-Miyaura Coupling: The Fork in the Trail

A. J. J. Lennox, G. C. Lloyd-Jones*

Angew. Chem. Int. Ed., 2013, 52, 7362-7370

[5] Preparation of Organotrifluoroborate Salts: Precipitation-Driven Equilibrium under Non-Etching Conditions

A. J. J. Lennox, G. C. Lloyd-Jones*

Angew. Chem. Int. Ed., 2012, 51, 9385-9388 VIP

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(Highlighted in RSC’s Chemistry World)

[4] R-BF3K Hydrolysis: Boronic Acid Release Mechanism and an Acid-Base Paradox in Cross-Coupling

A. J. J. Lennox, G. C. Lloyd-Jones*

J. Am. Chem. Soc., 2012, 134, 7431-7441

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(Highlighted in RSC’s Chemistry World)

[3] [(RCN)2PdCl2] - Catalyzed Isomerization of Alkenes: a Non-Hydride Binuclear Addition-Elimination Pathway

E. H. P. Tan, G. C. Lloyd-Jones,* J. N. Harvey,* A. J. J. Lennox, B. M. Mills,

Angew. Chem. Int. Ed., 2011, 50, 9602-9606

[2] The Slow-Release Strategy in Suzuki-Miyaura Coupling

A. J. J. Lennox, G. C. Lloyd-Jones*

Isr. J. Chem., 2010, 50, 664-674 (Invited contribution to Nobel Prize Issue)

[1] Aryl Trifluoroborates in Suzuki-Miyaura Coupling: The Roles of Endogenous Aryl Boronic Acid & Fluoride

M. Butters, J. N. Harvey, J. Jover, A. J. J. Lennox, G. C. Lloyd-Jones,* P. M. Murray
Angew. Chem. Int. Ed., 2010, 49, 5156-5160 (“Hot paper” and featured in C&E News)