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Clément Ghiazza
Clément Ghiazza
Institut Lavoisier Versailles ILV - CNRS
Dirección de correo verificada de uvsq.fr
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Visible‐Light‐Mediated Metal‐Free Synthesis of Trifluoromethylselenolated Arenes
C Ghiazza, V Debrauwer, C Monnereau, L Khrouz, M Médebielle, ...
Angewandte Chemie International Edition 57 (36), 11781-11785, 2018
782018
Synthetic approaches to trifluoromethylselenolated compounds
A Tlili, E Ismalaj, Q Glenadel, C Ghiazza, T Billard
Chemistry–A European Journal 24 (15), 3659-3670, 2018
742018
Visible-light promoted fluoroalkylselenolation: toward the reactivity of unsaturated compounds
C Ghiazza, L Khrouz, C Monnereau, T Billard, A Tlili
Chemical communications 54 (71), 9909-9912, 2018
652018
Copper‐Catalyzed Direct Trifluoro‐and Perfluoroalkylselenolations of Boronic Acids with a Shelf‐Stable Family of Reagents
Q Glenadel, C Ghiazza, A Tlili, T Billard
Advanced Synthesis & Catalysis 359 (19), 3414-3420, 2017
602017
Merging Visible‐Light Catalysis for the Direct Late‐Stage Group‐16–Trifluoromethyl Bond Formation
C Ghiazza, T Billard, A Tlili
Chemistry–A European Journal 25 (26), 6482-6495, 2019
562019
Trifluoromethyl‐and Fluoroalkylselenolations of Alkynyl Copper (I) Compounds
C Ghiazza, T Billard, A Tlili
Chemistry–A European Journal 23 (42), 10013-10016, 2017
392017
Exploring the reactivity of trifluoromethyl tolueneselenosulfonate with alkynes under copper catalysis
C Ghiazza, V Debrauwer, T Billard, A Tlili
Chemistry–A European Journal 24 (1), 97-100, 2018
382018
Chalcogen OCF3 Isosteres modulate drug properties without introducing inherent liabilities
C Ghiazza, T Billard, C Dickson, A Tlili, CM Gampe
ChemMedChem 14 (17), 1586-1589, 2019
352019
New avenues in radical trifluoromethylselenylation with trifluoromethyl tolueneselenosulfonate
C Ghiazza, C Monnereau, L Khrouz, M Médebielle, T Billard, A Tlili
Synlett 30 (07), 777-782, 2019
352019
Electrophilic trifluoromethylselenolation of terminal alkynes with Se-(trifluoromethyl) 4-methylbenzenesulfonoselenoate
C Ghiazza, A Tlili, T Billard
Beilstein Journal of Organic Chemistry 13 (1), 2626-2630, 2017
282017
Trifluoromethylselenolation and fluoroalkylselenolation of alkenes by electrophilic addition
C Ghiazza, Q Glenadel, A Tlili, T Billard
European Journal of Organic Chemistry 2017 (26), 3812-3814, 2017
272017
Electrophilic trifluoromethylselenolation of boronic acids
C Ghiazza, A Tlili, T Billard
Molecules 22 (5), 833, 2017
272017
Deaminative chlorination of aminoheterocycles
C Ghiazza, T Faber, A Gómez-Palomino, J Cornella
Nature Chemistry 14 (1), 78-84, 2022
262022
Strain‐Release Pentafluorosulfanylation and Tetrafluoro (aryl) sulfanylation of [1.1. 1] Propellane: Reactivity and Structural Insight
Y Kraemer, C Ghiazza, AN Ragan, S Ni, S Lutz, EK Neumann, ...
Angewandte Chemie 134 (48), e202211892, 2022
242022
Fluoroalkylselenolation of Alkyl Silanes/Trifluoroborates under Metal‐Free Visible‐Light Photoredox Catalysis
C Ghiazza, L Khrouz, T Billard, C Monnereau, A Tlili
European Journal of Organic Chemistry 2020 (10), 1559-1566, 2020
242020
Copper-promoted/copper-catalyzed trifluoromethylselenolation reactions
C Ghiazza, A Tlili
Beilstein Journal of Organic Chemistry 16 (1), 305-316, 2020
242020
Umpolung Reactivity of Fluoroalkylselenotoluenesulfonates: Towards a Versatile Reagent
C Ghiazza, A Kataria, A Tlili, F Toulgoat, T Billard
Asian Journal of Organic Chemistry 8 (5), 675-678, 2019
212019
Direct α‐C–H Trifluoromethylselenolation of Carbonyl Compounds
C Ghiazza, A Tlili, T Billard
European Journal of Organic Chemistry 2018 (27-28), 3680-3683, 2018
202018
Difluoro(aryl)(perfluoroalkyl)‐λ4‐sulfanes and Selanes: Missing Links of Trichloroisocyanuric Acid/Potassium Fluoride Chemistry
F Brüning, CR Pitts, J Kalim, D Bornemann, C Ghiazza, J de Montmollin, ...
Angewandte Chemie International Edition 58 (52), 18937-18941, 2019
192019
Regioselective remote CH fluoroalkylselenolation of 8-aminoquinolines
C Ghiazza, M Ndiaye, A Hamdi, A Tlili, T Billard
Tetrahedron 74 (45), 6521-6526, 2018
192018
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
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