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2020.
Radical reactivity of frustrated Lewis pairs with diaryl esters.
Cell Reports Physical Science
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Soltani, Yashar, Adams, Samuel J., Boerger, Jennifer, Wilkins, Lewis C., Newman, Paul D. ORCID: https://orcid.org/0000-0002-1808-1211, Pope, Simon J. A. ORCID: https://orcid.org/0000-0001-9110-9711 and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831
2018.
Synthesis and photophysical properties of imine borane adducts towards vapochromic materials.
Dalton Transactions
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10.1039/C8DT03019G
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Hokamp, Tobias, Mollari, Leonardo, Wilkins, Lewis C., Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831 and Wirth, Thomas ORCID: https://orcid.org/0000-0002-8990-0667
2018.
Alternative strategies with iodine: fast access to previously inaccessible iodine(III) compounds.
Angewandte Chemie International Edition
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Wilkins, Lewis C., Soltani, Yashar, Lawson, James R., Slater, Ben and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831
2018.
Divergent elementoboration: 1,3-haloboration versus 1,1-carboboration of propargyl esters.
Chemistry - A European Journal
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Melen, Rebecca ORCID: https://orcid.org/0000-0003-3142-2831, Soltani, Yashar and Wilkins, Lewis
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A comparative assessment of modern cyclization methods of substituted alkynyl esters, ethers, and acids.
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Wilkins, Lewis C., Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831, Platts, James A. ORCID: https://orcid.org/0000-0002-1008-6595 and Newman, Paul D. ORCID: https://orcid.org/0000-0002-1808-1211
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Amidine functionalized phosphines: tuneable ligands for transition metals.
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Soltani, Yashar, Wilkins, Lewis C. and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831
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Stoichiometric and catalytic C-C and C-H bond formation with B(C6F5)3 via cationic intermediates.
Angewandte Chemie International Edition
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Small molecule activation with frustrated Lewis pairs.
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Stöchiometrische und katalytische C-C- und C-H-Bindungsbildung mit B(C6
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Investigations into the photophysical and electronic properties of pnictoles and Their pnictenium counterparts.
Organometallics
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2017.
Supramolecular aggregation in dithia-arsoles: chlorides, cations and N-centred paddlewheels.
Crystengcomm
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Reactions of biologically inspired hydride sources with B(C6F5)3.
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Tris(2,4,6-trifluorophenyl)borane: an efficient hydroboration catalyst.
Chemistry - a European Journal
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Wilkins, Lewis C., Howard, Joseph L., Burger, Stefan, Frentzel-Beyme, Louis, Browne, Duncan L. ORCID: https://orcid.org/0000-0002-8604-229X and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831
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Exploring multistep continuous-flow hydrosilylation reactions catalyzed by tris(pentafluorophenyl)borane.
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Wilkins, Lewis
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Hard versus soft reactivity of Lewis acidic boranes.
PhD Thesis,
Cardiff University.
Item availability restricted. |
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Synthesis and reactivity of N,N’-1,4-diazabutadiene derived borocations.
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Enantioselective main group catalysis: modern catalysts for organic transformations.
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The propargyl rearrangement to functionalised allyl-boron and borocation compounds.
Chemistry - a European Journal
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Gegensätzliche Reaktivität frustrierter Lewis-Paare mit Selen- und Bor-basierten Lewis-Säuren.
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Contrasting frustrated Lewis pair reactivity with selenium- and boron-based Lewis acids.
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Pathways to functionalized heterocycles: propargyl rearrangement using B(C6F5)3.
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Lewis acid-base 1,2-addition reactions: synthesis of pyrylium borates from en-ynoate precursors.
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Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831, Wilkins, Lewis, Kariuki, Benson ORCID: https://orcid.org/0000-0002-8658-3897, Wadepohl, Hubert, Gade, Lutz, Hashmi, Stephen, Stephan, Douglas and Hansmann, Max
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Diverging pathways in the activation of allenes with Lewis acids and bases: addition, 1,2-Carboboration, and cyclization.
Organometallics
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Bähr, Alexander, Wilkins, Lewis, Ollegott, Kevin, Kariuki, Benson ORCID: https://orcid.org/0000-0002-8658-3897 and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831
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σ- versus π-activation of alkynyl benzoates using B(C6F5)3.
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