Soltani, Yashar, Dasgupta, Ayan, Gazis, Theodore A., Ould, Darren M.C., Richards, Emma ORCID: https://orcid.org/0000-0001-6691-2377, Slater, Ben, Stefkova, Katarina, Vladimirov, Vladimir Y., Wilkins, Lewis C., Willcox, Darren and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831 2020. Radical reactivity of frustrated Lewis pairs with diaryl esters. Cell Reports Physical Science 1 (2) 10.1016/j.xcrp.2020.100016 |
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 47 (36) , pp. 12656-12660. 10.1039/C8DT03019G |
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 57 (27) , pp. 8306-8309. 10.1002/anie.201804642 |
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 24 (29) , pp. 7364-7368. 10.1002/chem.201801493 |
Melen, Rebecca ORCID: https://orcid.org/0000-0003-3142-2831, Soltani, Yashar and Wilkins, Lewis 2017. A comparative assessment of modern cyclization methods of substituted alkynyl esters, ethers, and acids. Synlett 29 (01) , 01-07. 10.1055/s-0036-1591862 |
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 2017. Amidine functionalized phosphines: tuneable ligands for transition metals. Dalton Transactions 46 (41) , pp. 14234-14243. 10.1039/C7DT03343E |
Soltani, Yashar, Wilkins, Lewis C. and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831 2017. Stoichiometric and catalytic C-C and C-H bond formation with B(C6F5)3 via cationic intermediates. Angewandte Chemie International Edition 56 (39) , pp. 11995-11999. 10.1002/anie.201704789 |
Wilkins, Lewis C. and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831 2017. Small molecule activation with frustrated Lewis pairs. Encyclopedia of Inorganic and Bioinorganic Chemistry, Wiley, pp. 1-24. (10.1002/9781119951438.eibc2520) |
Soltani, Yashar, Wilkins, Lewis C. and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831 2017. Stöchiometrische und katalytische C-C- und C-H-Bindungsbildung mit B(C6 F5 )3 über kationische Zwischenstufen. Angewandte Chemie 129 (39) , pp. 12157-12161. 10.1002/ange.201704789 |
Ould, Darren M. C., Rigby, Alex C., Wilkins, Lewis C., Adams, Samuel J., Platts, James A. ORCID: https://orcid.org/0000-0002-1008-6595, Pope, Simon J. A. ORCID: https://orcid.org/0000-0001-9110-9711, Richards, Emma ORCID: https://orcid.org/0000-0001-6691-2377 and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831 2017. Investigations into the photophysical and electronic properties of pnictoles and Their pnictenium counterparts. Organometallics 37 (5) , pp. 712-719. 10.1021/acs.organomet.7b00564 |
Tran, Thao T. P., Ould, Darren M. C., Wilkins, Lewis C., Wright, Dominic S., Melen, Rebecca ORCID: https://orcid.org/0000-0003-3142-2831 and Rawson, Jeremy M. 2017. Supramolecular aggregation in dithia-arsoles: chlorides, cations and N-centred paddlewheels. Crystengcomm 19 (32) , pp. 4696-4699. 10.1039/C7CE01117B |
Wilkins, Lewis C., Santi, Nicolo ORCID: https://orcid.org/0000-0001-6361-5457, Luk, Louis Y. P. ORCID: https://orcid.org/0000-0002-7864-6261 and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831 2017. Reactions of biologically inspired hydride sources with B(C6F5)3. Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 375 (2101) , 20170009. 10.1098/rsta.2017.0009 |
Lawson, James, Wilkins, Lewis and Melen, Rebecca ORCID: https://orcid.org/0000-0003-3142-2831 2017. Tris(2,4,6-trifluorophenyl)borane: an efficient hydroboration catalyst. Chemistry - a European Journal 23 (46) , pp. 10997-11000. 10.1002/chem.201703109 |
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 2017. Exploring multistep continuous-flow hydrosilylation reactions catalyzed by tris(pentafluorophenyl)borane. Advanced Synthesis and Catalysis 359 (15) , pp. 2580-2584. 10.1002/adsc.201700349 |
Wilkins, Lewis
2017.
Hard versus soft reactivity of Lewis acidic boranes.
PhD Thesis,
Cardiff University.
Item availability restricted. |
Lawson, James, Wilkins, Lewis, Andre, Manon, Richards, Emma, Ali, Mohammed, Platts, James A. and Melen, Rebecca ORCID: https://orcid.org/0000-0003-3142-2831 2016. Synthesis and reactivity of N,N’-1,4-diazabutadiene derived borocations. Dalton Transactions 45 (41) , pp. 16177-16181. 10.1039/C6DT03360A |
Wilkins, Lewis C. and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831 2016. Enantioselective main group catalysis: modern catalysts for organic transformations. Coordination Chemistry Reviews 324 , pp. 123-139. 10.1016/j.ccr.2016.07.011 |
Wilkins, Lewis C., Lawson, James R., Wieneke, Philipp, Rominger, Frank, Hashmi, A. Stephen K., Hansmann, Max M. and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831 2016. The propargyl rearrangement to functionalised allyl-boron and borocation compounds. Chemistry - a European Journal 22 (41) , pp. 14618-14624. 10.1002/chem.201602719 |
Wilkins, Lewis C., Gunther, Benjamin A. R., Walther, Melanie, Lawson, James R., Wirth, Thomas ORCID: https://orcid.org/0000-0002-8990-0667 and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831 2016. Contrasting frustrated Lewis pair reactivity with selenium- and boron-based Lewis acids. Angewandte Chemie International Edition 55 (37) , pp. 11292-11295. 10.1002/anie.201605239 |
Wilkins, Lewis, Günther, Benjamin A.R., Walther, Melanie, Lawson, James, Wirth, Thomas ORCID: https://orcid.org/0000-0002-8990-0667 and Melen, Rebecca ORCID: https://orcid.org/0000-0003-3142-2831 2016. Gegensätzliche Reaktivität frustrierter Lewis-Paare mit Selen- und Bor-basierten Lewis-Säuren. Angewandte Chemie 128 (37) , pp. 11462-11465. 10.1002/ange.201605239 |
Wilkins, Lewis, Wieneke, Philipp, Newman, Paul David ORCID: https://orcid.org/0000-0002-1808-1211, Kariuki, Benson ORCID: https://orcid.org/0000-0002-8658-3897, Rominger, Frank, Hashmi, Sephen, Hansmann, Max and Melen, Rebecca L. ORCID: https://orcid.org/0000-0003-3142-2831 2015. Pathways to functionalized heterocycles: propargyl rearrangement using B(C6F5)3. Organometallics 34 (21) , pp. 5298-5309. 10.1021/acs.organomet.5b00753 |
Wilkins, Lewis, Hamilton, Hugh, Kariuki, Benson ORCID: https://orcid.org/0000-0002-8658-3897, Hashmi, Stephen, Hansmann, Max and Melen, Rebecca ORCID: https://orcid.org/0000-0003-3142-2831 2015. Lewis acid-base 1,2-addition reactions: synthesis of pyrylium borates from en-ynoate precursors. Dalton Transactions 45 , pp. 5929-5932. 10.1039/C5DT03340C |
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 2015. Diverging pathways in the activation of allenes with Lewis acids and bases: addition, 1,2-Carboboration, and cyclization. Organometallics 34 (16) , pp. 4127-4137. 10.1021/acs.organomet.5b00546 |
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 2015. σ- versus π-activation of alkynyl benzoates using B(C6F5)3. Molecules 20 (3) , pp. 4530-4547. 10.3390/molecules20034530 |