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Fady Nahra
Fady Nahra
Ghent University, Flemish Institute for Technological Research
Verified email at ugent.be - Homepage
Title
Cited by
Cited by
Year
Copper–NHC complexes in catalysis
F Lazreg, F Nahra, CSJ Cazin
Coordination Chemistry Reviews 293, 48-79, 2015
2232015
Striking AcOH acceleration in direct intramolecular allylic amination reactions
F Nahra, F Liron, G Prestat, C Mealli, A Messaoudi, G Poli
Chemistry–A European Journal 15 (42), 11078-11082, 2009
1212009
Copper/palladium-catalyzed 1, 4 reduction and asymmetric allylic alkylation of α, β-unsaturated ketones: enantioselective dual catalysis.
F Nahra, Y Macé, D Lambin, O Riant
Angewandte Chemie 125 (11), 2013
1182013
Palladium (0)-catalyzed difunctionalization of 1, 3-dienes: from racemic to enantioselective
X Wu, LZ Gong
Synthesis 51 (01), 122-134, 2019
1152019
Hydrofluorination of alkynes catalysed by gold bifluorides
F Nahra, SR Patrick, D Bello, M Brill, A Obled, DB Cordes, AMZ Slawin, ...
ChemCatChem 7 (2), 240-244, 2015
1042015
Exploring the coordination of cyclic selenoureas to gold (I)
DJ Nelson, F Nahra, SR Patrick, DB Cordes, AMZ Slawin, SP Nolan
Organometallics 33 (13), 3640-3645, 2014
932014
Copper (I) Complexes Bearing Carbenes Beyond Classical N‐Heterocyclic Carbenes: Synthesis and Catalytic Activity in “Click Chemistry”
YD Bidal, M Lesieur, M Melaimi, F Nahra, DB Cordes, ...
Advanced Synthesis & Catalysis 357 (14‐15), 3155-3161, 2015
832015
Mechanistic insight into the (NHC) copper (I)-catalyzed hydrosilylation of ketones
T Vergote, F Nahra, A Merschaert, O Riant, D Peeters, T Leyssens
Organometallics 33 (8), 1953-1963, 2014
822014
Synthesis and pharmacological evaluation of carboxycoumarins as a new antitumor treatment targeting lactate transport in cancer cells
N Draoui, O Schicke, A Fernandes, X Drozak, F Nahra, A Dumont, ...
Bioorganic & medicinal chemistry 21 (22), 7107-7117, 2013
802013
CuI/Pd0 Cooperative Dual Catalysis: Tunable Stereoselective Construction of Tetra‐Substituted Alkenes
S Vercruysse, L Cornelissen, F Nahra, L Collard, O Riant
Chemistry–A European Journal 20 (7), 1834-1838, 2014
742014
Copper (I)–NHC complexes as NHC transfer agents
F Nahra, A Gómez-Herrera, CSJ Cazin
Dalton Transactions 46 (3), 628-631, 2017
662017
Unprecedented copper (I) bifluoride complexes: synthesis, characterization and reactivity
T Vergote, F Nahra, A Welle, M Luhmer, J Wouters, N Mager, O Riant, ...
Chemistry–A European Journal 18 (3), 793-798, 2012
652012
A simple synthetic entryway into palladium cross-coupling catalysis
CM Zinser, F Nahra, M Brill, RE Meadows, DB Cordes, AMZ Slawin, ...
Chemical communications 53 (57), 7990-7993, 2017
622017
[Pd (NHC)(μ-Cl) Cl] 2: versatile and highly reactive complexes for cross-coupling reactions that avoid formation of inactive Pd (I) off-cycle products
T Zhou, S Ma, F Nahra, AMC Obled, A Poater, L Cavallo, CSJ Cazin, ...
Iscience 23 (8), 2020
612020
A mechanistically and operationally simple route to metal–N‐heterocyclic carbene (NHC) complexes
NV Tzouras, F Nahra, L Falivene, L Cavallo, M Saab, K Van Hecke, ...
Chemistry–A European Journal 26 (20), 4515-4519, 2020
612020
Synthesis of N-heterocyclic carbene gold (I) complexes
F Nahra, NV Tzouras, A Collado, SP Nolan
Nature Protocols 16 (3), 1476-1493, 2021
562021
POM@ IL-MOFs–inclusion of POMs in ionic liquid modified MOFs to produce recyclable oxidation catalysts
S Abednatanzi, K Leus, PG Derakhshandeh, F Nahra, K De Keukeleere, ...
Catalysis Science & Technology 7 (7), 1478-1487, 2017
562017
Conducting olefin metathesis reactions in air: Breaking the paradigm
S Guidone, O Songis, F Nahra, CSJ Cazin
ACS Catalysis 5 (5), 2697-2701, 2015
562015
Understanding existing and designing novel synthetic routes to Pd-PEPPSI-NHC and Pd-PEPPSI-PR 3 pre-catalysts
SG Guillet, VA Voloshkin, M Saab, M Beliš, K Van Hecke, F Nahra, ...
Chemical communications 56 (44), 5953-5956, 2020
452020
Sequential Functionalization of Alkynes and Alkenes Catalyzed by Gold (I) and Palladium (II) N‐Heterocyclic Carbene Complexes
A Gómez‐Herrera, F Nahra, M Brill, SP Nolan, CSJ Cazin
ChemCatChem 8 (21), 3381-3388, 2016
442016
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