Full publication list
118. Borane-Mediated Highly Secondary Selective Deoxyfluorination of Alcohols, Angew. Chem. Int. Ed. ASAP, 2024
Dominic R. Willcox, Nojus Cironis, Laura Winfrey, Sven Kirschner, Gary S. Nichol, Stephen P. Thomas*, and Michael J. Ingleson*
117. VIP paper! A Base-Free Two-Coordinate Oxoborane, Angew. Chem. Int. Ed. 2024, e202419094.
Clement R. P. Millet, Dominic R. Willcox, Gary S. Nichol, Cate S. Anstöter, Michael Ingleson*.
116. N-Directed Two-Fold Bromoboration of Diynes Enables Access to Brominated BN-Embedded PAHs. Org. Lett. 2024, ASAP
Xiaoran Feng, Zhaobo Liu, Qing-Yun Ni, Bing Wang*, Michael Ingleson, Kang Yuan*
115. Hot Paper! Transition Metal-Free Catalytic C−H Zincation and Alumination, Angew. Chem. Int. Ed. 2024, anie.202404848
Milan Kumar Bisai, Justyna Łosiewicz, Lia Sotorrios, Gary S. Nichol, Andrew P. Dominey, Michael J. Cowley, Stephen P. Thomas, Stuart A. Macgregor* and Michael J. Ingleson*
https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.202404848
114. Borylation–Reduction–Borylation for the Formation of 1,4-Azaborines. Org. Lett. 2023, ASAP
Shantaram S. Kothavale, Saqib A. Iqbal, Emily L. Hanover, Abhishek K. Gupta, Eli Zysman-Colman* and Michael J. Ingleson*
https://pubs.acs.org/doi/10.1021/acs.orglett.3c03731
113. NacNac-zinc-pyridonate mediated ε-caprolactone ROP. Dalton Trans. 2023, 52, 17767-17775
Jack W. J. Hughes , Dawid J. Babula , Findlay Stowers-Veitch , Kang Yuan , Marina Uzelac, Gary S. Nichol, Michael J. Ingleson* and Jennifer A. Garden*
https://pubs.rsc.org/en/content/articlehtml/2023/dt/d3dt03344a
112. Borylation directed borylation of N-alkyl anilines using iodine activated pyrazaboles. Chem. Sci. 2023, 14, 12041
C. R. P. Millet, E. Noone, A. V. Schellbach, J. Pahl, J. Łosiewicz, G. S. Nichol and M. J. Ingleson.
111. Brominated B1-Polycyclic Aromatic Hydrocarbons for the Synthesis of Deep-Red to Near-Infrared Delayed Fluorescence Emitters. Org. Lett. 2023 25, 5880–5884
K. Yuan, A. K. Gupta, C. Si, M. Uzelac, E. Zysman-Colman* and M. J. Ingleson*
https://pubs.acs.org/doi/10.1021/acs.orglett.3c02167
110. Main Group Catalyzed Arene Borylation: Challenges and Opportunities, ACS Catalysis, 2023, 13, 7691
M. J. Ingleson*
https://pubs.acs.org/doi/10.1021/acscatal.3c01668
109. Amides as Modifiable Directing Groups in Electrophilic Borylation, Chem. Sci. 2023, 14, 3865
S.. A. Iqbal, M. Uzelac, I. Nawaz, Z. Wang, T. H. Jones, K. Yuan, C. R. P. Millet, G. S. Nichol, G. Abbas Chotana and M. J. Ingleson*
https://pubs.rsc.org/en/content/articlepdf/2023/SC/D2SC06483A?page=search
108. Haloboration of o-Alkynyl Phenols Generates Halogenated Bicyclic-Boronates. Angew. Chem. Int. Ed. 2023, 62, e202301463
K. Yuan and M. J. Ingleson.*
https://onlinelibrary.wiley.com/doi/10.1002/anie.202301463
107. Understanding and Expanding Zinc Cation/Amine Frustrated Lewis Pair Catalyzed C–H Borylation. ACS Catalysis, 2023, 13, 2286–2294
M. E. Grundy, L. Sotorrios, M. Kumar Bisai, K. Yuan, S. A. Macgregor*, M. J. Ingleson*
106. Two Directing Groups Used for Metal Catalysed Meta-C–H Functionalisation Only Effect Ortho Electrophilic C–H Borylation. Special edition on Boron Chemistry in Eur. J. Org. Chem, 2022, ASAP.
S. A. Iqbal, C. R. P. Millet, J. Pahl, K. Yuan and M. J. Ingleson*.
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.202200901
105. Synthesis of Electrophiles Derived from Dimeric Aminoboranes and Assessing Their Utility in the Borylation of π Nucleophiles. Organometallics, 2022, 41, 2638
C. R. P. Millet, J. Pahl, E. Noone, K. Yuan, G. S. Nichol, M. Uzelac, M. J. Ingleson*
https://pubs.acs.org/doi/10.1021/acs.organomet.2c00393
104. Borylation Directed Borylation of Indoles Using Pyrazabole Electrophiles: A One-Pot Route to C7-Borylated-Indolines. Angew. Chem. Int. Ed. 2022, e202206230
J. Pahl, E. Noone, M. Uzelac, K. Yuan, M. J. Ingleson*
https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.202206230
103. XtalFluor-E effects the C3-H sulfenylation of indolesto form di-indole sulfides. Eur. J. Org. Chem. 2022, e202101394 (Special Edition on EaStChem researchers)
N. Cironis, K. Yuan, S. P. Thomas*, M. J. Ingleson*
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.202101394
102. Developing Organoboranes as phase transfer catalysts for nucleophilic fluorination using CsF. Chem. Sci. 2022, 13, 2661
S. Kirschner, M. Peters, K. Yuan, M. Uzelac and M. J. Ingleson
101. Enhanced N-directed electrophilic C-H borylation generates BN- [5]- and [6]helicenes with improved photophysical properties. Chem. Sci. 2022, 13, 1136
K. Yuan, D. Volland, S. Kirschner, M. Uzelac, G. S. Nichol, A. Nowak-Król* and M. J. Ingleson*
100. Formation of a hydride containing amido-zincate using pinacolborane. Dalton Trans. 2021, 50, 14018-14026
M. Uzelac, K. Yuan, G. S. Nichol, M. J. Ingleson.
https://pubs.rsc.org/en/content/articlelanding/2021/DT/D1DT02580E#!divAbstract
99. Zinc catalysed electrophilic C–H borylation of heteroarenes. Chem. Sci. 2021, 12, 8190
M. E. Grundy, K. Yuan, G. S. Nichol, M. J. Ingleson
https://pubs.rsc.org/en/content/articlelanding/2021/sc/d1sc01883c#!divAbstract
98. Controlling Selectivity in N-Heterocycle Directed Borylation of Indoles
S. A. Iqbal, K. Yuan, J. Cid, J. Pahl and M. J. Ingleson, Org. Biomol. Chem., 2021, 19, 2949
https://pubs.rsc.org/en/content/articlelanding/2021/ob/d1ob00018g#!divAbstract
97. Haloboration: scope, mechanism and utility. S. Kirschner, K. Yuan and M. J. Ingleson* New. J. Chem. 2020 Adv. Article
https://pubs.rsc.org/en/content/articlelanding/2020/nj/d0nj02908d#!divAbstract
96. Intramolecular (directed) electrophilic C-H borylation. S. A. Iqbal, J. Pahl, K. Yuan, M. J. Ingleson, Chem. Soc. Rev., 2020, 49, 4564
https://pubs.rsc.org/en/content/articlelanding/2020/cs/c9cs00763f#!divAbstract
95. A Comparison of Two Zinc Hydride Catalysts for Terminal Alkyne C–H Borylation/Hydroboration and the Formation of 1,1,1-Triborylalkanes by Tandem Catalysis Using Zn–H and B–H Compounds. M. Uzelac, K. Yuan, M. J. Ingleson*, Organometallics, 2020, 39, 8, 1332–1338
https://pubs.acs.org/doi/abs/10.1021/acs.organomet.0c00086
94. The Synthesis of Brominated-Boron-Doped PAHs by Alkyne 1,1-Bromoboration: Mechanistic and Functionalisation Studies. K. Yuan, R. J. Kahan, C. Si, A. Williams, M. Uzelac, E. Zysman-Colman* and M. J. Ingleson* Chem. Sci., 2020, 11, 3258-3267
http://dx.doi.org/10.1039/C9SC05404A - Open Access
93. In vivo optical performance of a new class of near infrared-emitting conjugated polymers: borylated PF8-BT. P. R. Neumann, D. L. Crossley, M. L. Turner, M. J. Ingleson, M. A. Green, J. Rao, L. A. Dailey. ACS Appl. Mater. Interfaces 2019, 11, 50, 46525-46535
https://pubs.acs.org/doi/10.1021/acsami.9b17022
92. Metal-free acyl-directed electrophilic C-H borylation using just BBr3. M. J. Ingleson. Science China Chemistry, 2019, 62, pages 1547–1548
https://link.springer.com/article/10.1007%2Fs11426-019-9642-0
91. Acyl Directed ortho‐Borylation of Anilines and C7 Borylation of Indoles using just BBr3. S. A. Iqbal, J. Cid, R. Procter, M. Uzelac, K. Yuan and M. J. Ingleson*. Angew. Chem. Int. Ed., 2019, 58, 15381
https://doi.org/10.1002/anie.201909786
90. Borylative cyclisation of diynes using BCl3 and borocations. Andrew J. Warner, K. M. Enright, J. M. Cole, K. Yuan, J. S. McGough, M. J. Ingleson*, Org. Biomol. Chem., 2019, 17, 5520-5525
https://pubs.rsc.org/en/content/articlelanding/2019/ob/c9ob00991d#!divAbstract
89. Low-Coordinate NHC-Zinc Hydride Complexes Catalyze Alkyne C-H Borylation and Hydroboration Using Pinacolborane. Richard J. Procter, Marina Uzelac, Jessica Cid, Philip J. Rushworth, Michael J. Ingleson* ACS Catal. 2019, 9, 5760-5771
https://pubs.acs.org/doi/full/10.1021/acscatal.9b01370
88. Well-Defined Boron/Nitrogen-Doped Polycyclic Aromatic Hydrocarbons Are Active Electrocatalysts for the Oxygen Reduction Reaction.Rachel J. Kahan, Wisit Hirunpinyopas, Jessica Cid, Michael J. Ingleson* and Robert A. W. Dryfe* Chem.Mater. 2019, 31, 1891−1898.
https://pubs.acs.org/doi/pdf/10.1021/acs.chemmater.8b04027
87. Benzoselenadiazole and benzotriazole directed electrophilic C-H borylation of conjugated donor-acceptor materials. B. Dash, I. Hamilton, D. J. Tate, D. L. Crossley, J.-S. Kim, M. J. Ingleson*, M. L. Turner*, J. Mater. Chem. C, 2019, 7, 718-724
https://pubs.rsc.org/en/Content/ArticleLanding/2018/TC/C8TC05131C#!divAbstract
86. Reductive α-borylation of α,β-unsaturated esters using NHC-BH3 activated by I2 as a metal-free route to α-boryl esters. J. E. Radcliffe, V. Fasano, R. W. Adams, P. You, M. J. Ingleson*. Chem. Sci., 2019,10, 1434
https://pubs.rsc.org/en/content/articlepdf/2014/SC/C8SC04305A?page=search
Phosphorous(V) Lewis Acids: Water-Base Tolerant P3-trimethylated trications. J. M. Bayne, V. Fasano, K. M. Szkop, M. J. Ingleson* and D. W. Stephan*. Chem. Comm. 2018, 54, 12467
https://pubs.rsc.org/en/content/articlelanding/2018/cc/c8cc06564k#!divAbstract
Selective boryl‐anion migration in a vinyl sp2‐sp3 diborane induced by soft borane Lewis acids. Valerio Fasano, Jessica Cid, Emily Ross, Richard Procter and Michael Ingleson* Angew. Chem. Int. Ed. 2018, 57, 13293
https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201808216
Generation of a series of Bn fused oligo-naphthalenes. (n = 1 to 3) from a B1-polycyclic aromatic hydrocarbon R. J. Kahan, D. L. Crossley, J. Cid, J. E. Radcliffe, A. W. Woodward, V. Fasano, S. Endres, G. F. S. Whitehead, M. J. Ingleson* Chem. Commun., 2018, 54, 9490
https://pubs.rsc.org/en/content/articlelanding/2018/cc/c8cc04701d#!divAbstract
Diboryldiborenes: p-Conjugated B4 Chains Isoelectronic to the Butadiene Dication; A. Hermann, J. Cid, J. D. Mattock, R. D. Dewhurst, I. Krummenacher, A. Vargas*, M. J. Ingleson*, H. Braunschweig* Angew. Chem. Int. Ed. 2018, 57, 10091
https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201805394
The Synthesis of Unsymmetrical Diboron(5) Compounds and their Conversion to Diboron(5) Cations. J. Cid, A. Hermann, J. Radcliffe, L. Curless, H. Braunschweig*, M. Ingleson, Organometallics, 2018, 37, 1992.
https://pubs.acs.org/doi/10.1021/acs.organomet.8b00288
C‐H Borylation / Cross Coupling Forms Twisted Donor‐Acceptor Compounds Exhibiting Donor Dependent Delayed Emission. D. Crossley, P. Kulapichitr, J. Radcliffe, J. Dunsford, R. J. Kahan, A. Woodward, I. Vitorica-Yrezabal, M. Turner*, J. McDouall* M. J. Ingleson*. Chem. Eur. J. 2018, 24, 10521.
https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.201801799
Synthesis, Characterization and Functionalization of 1-Bora-phenalenes. R. J. Kahan, D. L. Crossley, J. Cid, J. E. Radcliffe, M. J. Ingleson*. Angew. Chem. Int. Ed., 2018, 57, 8084
https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201803180
Recent Advances in Water-Tolerance in Frustrated Lewis Pair Chemistry. V. Fasano, M. J. Ingleson*, Synthesis, 2018, 50, 1783.
https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0037-1609843
Air– and water–stable Lewis acid: synthesis and reactivity of P-trifluoromethyl electrophilic phosphonium cations. V. Fasano, J. H. W. LaFortune, J. M. Bayne, M. J. Ingleson*, D. W. Stephan*, Chem. Comm., 2018, 54, 662.
http://pubs.rsc.org/en/Content/ArticleLanding/2018/CC/C7CC09128A#!divAbstract
N-Heterocycle-Ligated Borocations as Highly Tunable Carbon Lewis Acids. J. E. Radcliffe, J. J. Dunsford, J. Cid, V. Fasano, M. J. Ingleson* Organometallics, 2017, 36, 4952.
http://pubs.acs.org/doi/abs/10.1021/acs.organomet.7b00779
A modular route to boron doped PAHs by combining borylative cyclisation and electrophilic C–H borylation. D. L. Crossley, R. J. Kahan, S. Endres, A. J. Warner, R. A. Smith, J. Cid, J. J. Dunsford, J. E. Jones, I. Vitorica-Yrezabal and M. J. Ingleson*. Chem. Sci., 2017,8, 7969
http://pubs.rsc.org/en/content/articlelanding/2017/sc/c7sc02793a#!divAbstract
A Zinc Catalyzed C(sp3)-C(sp2) Suzuki-Miyaura Cross-Coupling Reaction Mediated by Aryl-Zincates. R. J. Procter, J. J. Dunsford, P. J. Rushworth, D. G. Hulcoop, R. A. Layfield, M. J. Ingleson*, Chem.Eur. J., 2017, 23, 15889
http://onlinelibrary.wiley.com/doi/10.1002/chem.201704170/epdf
Post-Polymerization C-H Borylation of Donor-Acceptor Materials Gives Highly Efficient Solid State Near-Infrared Emitters for NIR-OLEDs and Effective Biological Imaging. D. L. Crossley, L. Urbano, R. P. Neumann, S. Bourke, J. Jones, L. A. Dailey*, M. Green, M. J. Humphries, S. King, M. L. Turner*, M. J. Ingleson*. Appl. Mater. Int. 2017, 9, 28243
http://pubs.acs.org/doi/pdf/10.1021/acsami.7b08473
Frustrated Lewis Pair Mediated 1,2-Hydrocarbation of Alkynes. V. Fasano, L. D. Curless, J. E. Radcliffe, M. J. Ingleson* Angew. Chem. Int. Ed., 2017, 56, 9202
http://onlinelibrary.wiley.com/doi/10.1002/anie.201705100/abstract
Use of N-methyliminodiacetic Acid Boronate Esters in Suzuki-Miyaura Cross-Coupling Polymerizations of Triarylamine and Fluorene Monomers. A. B. Foster, V. Bagutski, J. I. Ayuso-Carrillo, M. J. Humphries, M. J. Ingleson, M. L. Turner* J. Poly. Sci. A. 2017, 55, 2798.
http://onlinelibrary.wiley.com/doi/10.1002/pola.28682/abstract
Catalytic Electrophilic C-H Borylation using NHC·Boranes and Iodine Forms C2-, not C3-, Borylated Indoles. J. McGough, J. Cid, M. J. Ingleson.* Chem. Eur. J., 2017, 23, 8180..
http://onlinelibrary.wiley.com/doi/10.1002/chem.201702060/full
Borylated Arylamine-Benzothiadiazole Donor-Acceptor Materials as Low LUMO, Low Band-Gap Chromophores D. L. Crossley, R. Goh, J. Cid, I. Vitorica-Yrezabal, M. L. Turner* and M. J. Ingleson*. Organometallics, 2017, 36, 2597
Organometallics: http://dx.doi.org/10.1021/acs.organomet.7b00188
Mechanistic Insights into the B(C6F5)3-Initiated Aldehyde–Aniline–Alkyne Reaction To Form Substituted Quinolines. V. Fasano, J. Radcliffe, M. J. Ingleson.* Organometallics, 2017, 36, 1623.
http://pubs.acs.org/doi/abs/10.1021/acs.organomet.7b00174
Expanding Water/Base Tolerant FLP Chemistry to Alkylamines Enables Broad Scope Reductive Aminations. V. Fasano, M. J. Ingleson*Chem. Eur. J., 2017, 23, 2217
http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201605466/abstract
BCl3-Induced Annulative Oxo- and Thioboration for the Formation of C3-Borylated Benzofurans and Benzothiophenes. A. J. Warner, A. Churn, J. S. McGough, M. J. Ingleson.* Angew. Chem. Int. Ed., 2017, 56, 354
http://onlinelibrary.wiley.com/wol1/doi/10.1002/anie.201610014/abstract
N-Methyl-Benzothiazolium Salts as Carbon Lewis Acids for Si−H σ-Bond Activation and Catalytic (De)hydrosilylation. V. Fasano, J. E. Radcliffe, L. D. Curless, M. J. Ingleson.* Chem. Eur. J., 2017, 23, 187.
Selected as a “hot paper”!
http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201604613/abstract
A General Protocol for the Polycondensation of Thienyl-MIDA Boronate Esters to Form High Molecular Weight Copolymers. J. Ayuso Carrillo, M. L. Turner*, M. J. Ingleson*, JACS, 2016, 138, 13361.
http://pubs.acs.org/doi/abs/10.1021/jacs.6b07666
Highly Emissive Far Red / Near-IR Fluorophores Based on Borylated Fluorene-Benzothiadiazole Donor-Acceptor Materials. D. L. Crossley, I. Vitorica-Yrezabal, M. J. Humphries, M. L. Turner*, M. J. Ingleson*. Chem. Eur. J., 2016, 22, 12439
http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201602010/abstract
Three-Coordinate Iron(II) Expanded Ring N-Heterocyclic Carbene Complexes. J. J. Dunsford, D. J. Evans, T. Pugh, S. N. Shah, N. F. Chilton*, M. J. Ingleson* Organometallics, 2016, 35, 1098
http://pubs.acs.org/doi/abs/10.1021/acs.organomet.6b00121
B(C6F5)3 Catalyzed Reductive Amination using Hydrosilanes. V. Fasano, J. E. Radcliffe, M. J. Ingleson* ACS Catal. 2016, 6, 1793.
http://pubs.acs.org/doi/abs/10.1021/acscatal.5b02896
Inter- and intra-molecular C–H borylation for the formation of PAHs containing triarylborane and indole units. A. Escande, D. L. Crossley, J. Cid, I. A. Cade, I. Vitorica-Yrezabal, M. J. Ingleson, Dalton Trans., 2016, 45, 17160.
http://pubs.rsc.org/en/Content/ArticleLanding/2016/DT/C6DT03526D#!divAbstract
Highly selective catalytic trans-hydroboration of alkynes mediated by borenium cations and B(C6F5)3. J. S. McGough, S. M. Butler, I. A. Cade, M. J. Ingleson* Chem. Sci., 2016, 7, 3384.
Selected as a “hot article”
http://pubs.rsc.org/en/Content/ArticleLanding/2016/SC/C5SC04798F#!divAbstract
Metal-free electrocatalytic hydrogen oxidation using frustrated Lewis pairs and carbon-based Lewis acids. E. J Lawrence, E., L. D. Curless, J. M. Courtney, R. J. Blagg, M. J. Ingleson* and G. G. Wildgoose* Chem. Sci., 2016, 7, 2357
http://pubs.rsc.org/en/content/articlelanding/2016/sc/c5sc04564a#!divAbstract
The carboboration of Me3Si-substituted alkynes and allenes with boranes and borocations. J. R. Lawson, V. Fasano, J. Cid, I. Vitorica-Yrezabal and M. J. Ingleson* Dalton Trans., 2016, 45, 6060.
http://pubs.rsc.org/en/Content/ArticleLanding/2015/DT/c5dt03003j#!divAbstract
Arylation of 4-Coordinate Boron Halides by Borenium Cation Mediated Boro-desilylation and –destannylation. D. L. Crossley, J. Cid, L. D. Curless, M. L. Turner, and M. J. Ingleson*. Organometallics, 2015, 34, 5767
http://pubs.acs.org/doi/abs/10.1021/acs.organomet.5b00857
Highly nucleophilic dipropanolamine chelated boron reagents for aryl-transmetallation to iron complexes. J. J. Dunsford, E. R. Clark and M. J. Ingleson* Dalton Trans., 2015, 44, 20577
http://pubs.rsc.org/en/content/articlelanding/2015/dt/c5dt03835a#!divAbstract
Formation of C(sp2)-Boronate Esters by Transition Metal-Free Borylative Cyclisation of Alkynes Using BCl3 . Angew, Chem. Int. Ed., 2015, 54, 11245, A. J. Warner, J. R. Lawson, V. Fasano and M. J. Ingleson*
One of the top accessed ACIE papers in August 2015 (its month of publication)
http://onlinelibrary.wiley.com/doi/10.1002/anie.201505810/abstract
Complete reductive cleavage of CO facilitated by highly electrophilic borocations Chem. Commun., 2015, 51, 10903, L. D. Curless, E. R. Clark, J. Cid, A. Del Grosso and M. J. Ingleson*
http://pubs.rsc.org/en/content/articlelanding/2015/cc/c5cc03504j?iscitedby=True#!divAbstract
Enhancing electron affinity and tuning band gap in donor–acceptor organic semiconductors by benzothiadiazole directed C–H borylation. Chem. Sci. 2015, 6, 5144, D. L. Crossley, I. A. Cade, E. R. Clark, A. Escande, M. J. Humphries, S. M. King, I. Vitorica-Yrezabal, M. J. Ingleson* and M. L. Turner*
http://pubs.rsc.org/en/content/articlehtml/2015/sc/c5sc01800e
Room Temperature Ring Expansion of N-Heterocyclic Carbenes and B-B Bond Cleavage of Diboron(4) Compounds. Chem. Eur, J., 2015, 21, 9018. S. Pietsch, U. Paul, I. A. Cade, M. J. Ingleson,* Udo Radius* and Todd B. Marder*
http://onlinelibrary.wiley.com/doi/10.1002/chem.201501498/abstract
1,1/1,2 Isomerisation in Lewis base adducts of B2cat2. Dalton Trans., 2015, 44, 7506. I. A. Cade, W. Y. Chau, I. Vitorica-Yrezabal and M. J. Ingleson*
http://pubs.rsc.org/en/Content/ArticleLanding/2015/DT/c5dt00645g#!divAbstract
Direct C(sp2)C(sp3) Cross-Coupling of Diaryl Zinc Reagents with Benzylic, Primary, Secondary, and Tertiary Alkyl Halides. Angew. Chem. Int. Ed., 2015, J. J Dunsford, E. R. Clark and M. J. Ingleson*
Selected as a VIP paper
http://onlinelibrary.wiley.com/doi/10.1002/anie.201411403/abstract
Fused polycyclic aromatics incorporating boron in the core: fundamentals and applications. Chem. Commun., 2015, 51, 6257. A. Escande and M. J. Ingleson.
http://pubs.rsc.org/en/content/articlelanding/2015/cc/c5cc00175g#!divAbstract
Thienyl MIDA Boronate Esters as Highly Effective Monomers for Suzuki-Miyaura Polymerization Reactions. Macromolecules, 2015, 48, 979. J. Ayuso Carrillo, M. J. Ingleson* and M. L. Turner*
http://pubs.acs.org/doi/abs/10.1021/ma502542g
Regioselective electrophilic borylation of haloarenes. Chem. Commun., 2015, 51, 979. A. Del Grosso, J. Ayuso Carrillo and M. J. Ingleson*
http://pubs.rsc.org/en/Content/ArticleLanding/2015/CC/c4cc10153g#!divAbstract
Fundamental and Applied Properties of Borocations. M. J. Ingleson. Book Chapter in Synthesis and Applications of Organoboron Compounds. Vol. 49 of Topics in Organometallic Chemistry. Pgs 39-71
B(C6F5)3 Catalyzed Synthesis of Benzofused Siloles. Organometallics, 2014, 33, 7241. L. D. Curless and M. J. Ingleson*
http://pubs.acs.org/doi/abs/10.1021/om501033p
N-Methylacridinium Salts: Carbon Lewis Acids in Frustrated Lewis Pairs for sigma bond activation and catalytic reductions. Angew. Chem. Int. Ed., 2014, 53, 11306. E. R. Clark and M. J. Ingleson.*
http://onlinelibrary.wiley.com/doi/10.1002/anie.201406122/abstract
syn-1,2-carboboration of Alkynes with Borenium Cations. Chemistry a European Journal, 2014, 20, 12874. I. A. Cade and M. J. Ingleson*
http://onlinelibrary.wiley.com/doi/10.1002/chem.201403614/abstract
Reactivity of (NHC)2FeX2 Complexes toward Arylborane Lewis Acids and Arylboronates. Organometallics, 2014, 33, 370, J. J. Dunsford, I. A. Cade, K. L. F., M. L. Neidig, and M. J. Ingleson *
http://pubs.acs.org/doi/abs/10.1021/om401105k
E–H (E = R3Si or H) bond activation by B(C6F5)3 and heteroarenes; competitive dehydrosilylation, hydrosilylation and hydrogenation. Chem. Commun., 2014, 50, 5270, L. D. Curless, E. R. Clark, J. J. Dunsford and M. J. Ingleson*
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