| Transition‐metal‐free diboration reaction by activation of diboron compounds with simple Lewis bases A Bonet, C Pubill‐Ulldemolins, C Bo, H Gulyás, E Fernández Angewandte Chemie International Edition 50 (31), 7158-7161, 2011 | 321 | 2011 |
| Activation of diboron reagents with Brønsted bases and alcohols: an experimental and theoretical perspective of the organocatalytic boron conjugate addition reaction C Pubill‐Ulldemolins, A Bonet, C Bo, H Gulyás, E Fernández Chemistry–A European Journal 18 (4), 1121-1126, 2012 | 165 | 2012 |
| Living GenoChemetics by hyphenating synthetic biology and synthetic chemistry in vivo SV Sharma, X Tong, C Pubill-Ulldemolins, C Cartmell, EJA Bogosyan, ... Nature communications 8 (1), 229, 2017 | 79 | 2017 |
| Essential role of phosphines in organocatalytic β-boration reaction C Pubill-Ulldemolins, A Bonet, H Gulyás, C Bo, E Fernández Organic & Biomolecular Chemistry 10 (48), 9677-9682, 2012 | 71 | 2012 |
| Nucleophilic boron strikes back H Gulyás, A Bonet, C Pubill-Ulldemolins, C Sole, J Cid, E Fernandez Pure and Applied Chemistry. Chimie Pure et Appliquee 84 (11), 2219, 2012 | 60 | 2012 |
| Metal-free borylative ring-opening of vinyl epoxides and aziridines X Sanz, GM Lee, C Pubill-Ulldemolins, A Bonet, H Gulyas, SA Westcott, ... Organic & Biomolecular Chemistry 11 (40), 7004-7010, 2013 | 55 | 2013 |
| A new context for palladium mediated B-addition reaction: an open door to consecutive functionalization C Pubill-Ulldemolins, A Bonet, C Bo, H Gulyás, E Fernández Organic & Biomolecular Chemistry 8 (12), 2667-2682, 2010 | 51 | 2010 |
| Sonogashira diversification of unprotected halotryptophans, halotryptophan containing tripeptides; and generation of a new to nature bromo-natural product and its … MJ Corr, SV Sharma, C Pubill-Ulldemolins, RT Bown, P Poirot, ... Chemical Science 8 (3), 2039-2046, 2017 | 49 | 2017 |
| Rhodium–NHC complexes mediate diboration versus dehydrogenative borylation of cyclic olefins: A theoretical explanation C Pubill-Ulldemolins, M Poyatos, C Bo, E Fernández Dalton Transactions 42 (3), 746-752, 2013 | 34 | 2013 |
| Perceptible Influence of Pd and Pt Heterocyclic Carbene–Pyridyl Complexes in Catalytic Diboration of Cyclic Alkenes C Pubill‐Ulldemolins, C Bo, JA Mata, E Fernández Chemistry–An Asian Journal 5 (2), 261-264, 2010 | 25 | 2010 |
| Bis (3, 5‐dimethyl‐4‐vinylpyrazol‐1‐yl) acetic Acid: A New Heteroscorpionate Building Block for Copolymers that Mimic the 2‐His‐1‐carboxylate Facial Triad G Türkoglu, C Pubill Ulldemolins, R Müller, E Hübner, FW Heinemann, ... European Journal of Inorganic Chemistry 2010 (19), 2962-2974, 2010 | 24 | 2010 |
| Origins of observed reactivity and specificity in the addition of B 2 Cl 4 and analogues to unsaturated compounds C Pubill-Ulldemolins, E Fernánez, C Bo, JM Brown Organic & Biomolecular Chemistry 13 (37), 9619-9628, 2015 | 20 | 2015 |
| Heck diversification of indole‐based substrates under aqueous conditions: from indoles to unprotected halo‐tryptophans and halo‐tryptophans in natural product derivatives C Pubill‐Ulldemolins, SV Sharma, C Cartmell, J Zhao, P Cárdenas, ... Chemistry–A European Journal 25 (46), 10866-10875, 2019 | 19 | 2019 |
| Buchwald Hartwig diversification of unprotected halotryptophans, halotryptophan containing tripeptides and the natural product barettin in aqueous conditions YJG Renault, R Lynch, E Marelli, SV Sharma, C Pubill-Ulldemolins, ... Chemical Communications 55 (91), 13653-13656, 2019 | 19 | 2019 |
| Skeletally tunable seven-membered-ring fused pyrroles D Andreou, NB Essien, C Pubill-Ulldemolins, MA Terzidis, ... Organic Letters 23 (17), 6685-6690, 2021 | 16 | 2021 |
| An expedient, mild and aqueous method for Suzuki–Miyaura diversification of (hetero) aryl halides or (poly) chlorinated pharmaceuticals SV Sharma, C Pubill-Ulldemolins, E Marelli, RJM Goss Organic Chemistry Frontiers 8 (20), 5722-5727, 2021 | 11 | 2021 |
| A One‐Pot Synthesis of Symmetrical and Unsymmetrical Dipeptide Ureas AA Fayad, C Pubill‐Ulldemolins, SV Sharma, D Day, RJM Goss European Journal of Organic Chemistry 2015 (25), 5603-5609, 2015 | 7 | 2015 |
| Developing a Bench-Scale Green Diboration Reaction toward Industrial Application A Farre, R Briggs, C Pubill-Ulldemolins, A Bonet Synthesis 49 (21), 4775-4782, 2017 | 2 | 2017 |
| JA SHARP, C. CARTMELL, P. CÁRDENAS, RJM GOSS*(UNIVERSITY OF ST ANDREWS, UK) YJG RENAULT, R LYNCH, E MARELLI, SV SHARMA, ... Chem. Commun 55, 13653-13656, 2019 | | 2019 |
| Selective functionalisation and diversification of halogenated compounds through mild aqueous cross-coupling methodologies: From organic molecules to natural products C Pubill-Ulldemolins, M Corr, S Sharma, E Marelli, R Goss ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 253, 2017 | | 2017 |
