Year |
Citation |
Score |
2023 |
Yang Y, Taponard A, Vantourout JC, Tlili A. Synthesis of Fluorinated Amines: A Personal Account. Acs Organic & Inorganic Au. 3: 364-370. PMID 38075451 DOI: 10.1021/acsorginorgau.3c00029 |
0.337 |
|
2023 |
Abid S, Quirion KP, Yang Y, Tang R, Mai BK, Liu P, Tlili A. Photochemically Driven Nickel-Catalyzed Carboxylative C-N Coupling: Scope and Mechanism. Chemistry (Weinheim An Der Bergstrasse, Germany). e202301271. PMID 37184082 DOI: 10.1002/chem.202301271 |
0.338 |
|
2020 |
Abou Derhamine S, Krachko T, Monteiro N, Pilet G, Schranck J, Tlili A, Amgoune A. Nickel-Catalyzed Mono-Selective α-Arylation of Acetone with Aryl Chlorides and Phenol Derivatives. Angewandte Chemie (International Ed. in English). PMID 32667110 DOI: 10.1002/Anie.202006826 |
0.363 |
|
2020 |
Ghiazza C, Tlili A. Copper-promoted/copper-catalyzed trifluoromethylselenolation reactions. Beilstein Journal of Organic Chemistry. 16: 305-316. PMID 32256848 DOI: 10.3762/Bjoc.16.30 |
0.331 |
|
2019 |
Onida K, Tlili A. Direct Synthesis of Carbamoyl Fluorides by CO Deoxyfluorination. Angewandte Chemie (International Ed. in English). 58: 12545-12548. PMID 31297908 DOI: 10.1002/Anie.201907354 |
0.444 |
|
2019 |
Ghiazza C, Billard T, Tlili A. Merging Visible-Light Catalysis for the Direct Late-Stage Group-16-Trifluoromethyl Bond Formation. Chemistry (Weinheim An Der Bergstrasse, Germany). 25: 6482-6495. PMID 30644601 DOI: 10.1002/Chem.201806234 |
0.387 |
|
2019 |
Onida K, Vanoye L, Tlili A. Direct Synthesis of Thiocarbamoyl Fluorides and Trifluoromethylamines Through Fluorinative Desulfurization European Journal of Organic Chemistry. 2019: 6106-6109. DOI: 10.1002/Ejoc.201901113 |
0.368 |
|
2019 |
Ghiazza C, Billard T, Tlili A. Frontispiece: Merging Visible‐Light Catalysis for the Direct Late‐Stage Group‐16–Trifluoromethyl Bond Formation Chemistry – a European Journal. 25. DOI: 10.1002/Chem.201982663 |
0.302 |
|
2019 |
Ghiazza C, Kataria A, Tlili A, Toulgoat F, Billard T. Umpolung Reactivity of Fluoroalkylselenotoluenesulfonates: Towards a Versatile Reagent Asian Journal of Organic Chemistry. 8: 675-678. DOI: 10.1002/Ajoc.201900027 |
0.338 |
|
2018 |
Pichette Drapeau M, Tlili A, Zaid Y, Toummini D, Ouazzani Chahdi F, Sotiropoulos JM, Ollevier T, Taillefer M. Transition-Metal-Free Synthesis of Biarylmethanes from Aryl Iodides and Benzylic Ketones. Chemistry (Weinheim An Der Bergstrasse, Germany). 24: 17449-17453. PMID 30169893 DOI: 10.1002/Chem.201804415 |
0.407 |
|
2018 |
Ghiazza C, Khrouz L, Monnereau C, Billard T, Tlili A. Visible-light promoted fluoroalkylselenolation: toward the reactivity of unsaturated compounds. Chemical Communications (Cambridge, England). 54: 9909-9912. PMID 30105319 DOI: 10.1039/C8Cc05256E |
0.35 |
|
2018 |
Ghiazza C, Debrauwer V, Monnereau C, Khrouz L, Médebielle M, Billard T, Tlili A. Visible-Light-Mediated Metal-Free Synthesis of Trifluoromethylselenolated Arenes. Angewandte Chemie (International Ed. in English). 57: 11781-11785. PMID 29985549 DOI: 10.1002/Anie.201806165 |
0.391 |
|
2018 |
Ghiazza C, Debrauwer V, Billard T, Tlili A. Exploring the Reactivity of Trifluoromethyl Tolueneselenosulfonate with Alkynes under Copper Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 24: 97-100. PMID 29152790 DOI: 10.1002/Chem.201705231 |
0.412 |
|
2018 |
Tlili A, Ismalaj E, Glenadel Q, Ghiazza C, Billard T. Synthetic Approaches to Trifluoromethylselenolated Compounds. Chemistry (Weinheim An Der Bergstrasse, Germany). 24: 3659-3670. PMID 29072337 DOI: 10.1002/Chem.201704637 |
0.319 |
|
2018 |
Ghiazza C, Monnereau C, Khrouz L, Médebielle M, Billard T, Tlili A. New Avenues in Radical Trifluoromethylselenylation with Trifluoromethyl Tolueneselenosulfonate Synlett. 30: 777-782. DOI: 10.1055/S-0037-1610347 |
0.38 |
|
2018 |
Ghiazza C, Monnereau C, Khrouz L, Billard T, Tlili A. Visible-Light-Mediated Synthesis of Trifluoromethylthiolated Arenes Synthesis. 51: 2865-2870. DOI: 10.1055/S-0037-1610322 |
0.398 |
|
2018 |
Ghiazza C, Ndiaye M, Hamdi A, Tlili A, Billard T. Regioselective remote C H fluoroalkylselenolation of 8-aminoquinolines Tetrahedron. 74: 6521-6526. DOI: 10.1016/J.Tet.2018.09.048 |
0.425 |
|
2018 |
Ghiazza C, Tlili A, Billard T. Cover Feature: Direct α-C-H Trifluoromethylselenolation of Carbonyl Compounds (Eur. J. Org. Chem. 27-28/2018) European Journal of Organic Chemistry. 2018: 3498-3498. DOI: 10.1002/Ejoc.201801028 |
0.35 |
|
2018 |
Ghiazza C, Tlili A, Billard T. Direct α-C-H Trifluoromethylselenolation of Carbonyl Compounds European Journal of Organic Chemistry. 2018: 3680-3683. DOI: 10.1002/Ejoc.201800237 |
0.36 |
|
2017 |
Ghiazza C, Tlili A, Billard T. Electrophilic trifluoromethylselenolation of terminal alkynes with -(trifluoromethyl) 4-methylbenzenesulfonoselenoate. Beilstein Journal of Organic Chemistry. 13: 2626-2630. PMID 29259673 DOI: 10.3762/Bjoc.13.260 |
0.411 |
|
2017 |
Ghiazza C, Billard T, Tlili A. Trifluoromethyl- and Fluoroalkylselenolations of Alkynyl Copper(I) Compounds. Chemistry (Weinheim An Der Bergstrasse, Germany). 23: 10013-10016. PMID 28635038 DOI: 10.1002/Chem.201702028 |
0.387 |
|
2017 |
Ghiazza C, Tlili A, Billard T. Electrophilic Trifluoromethylselenolation of Boronic Acids. Molecules (Basel, Switzerland). 22. PMID 28534838 DOI: 10.3390/Molecules22050833 |
0.41 |
|
2017 |
Schranck J, Tlili A. Transition-Metal-Catalyzed Monoarylation of Ammonia Acs Catalysis. 8: 405-418. DOI: 10.1021/Acscatal.7B03215 |
0.357 |
|
2017 |
Schranck J, Furer P, Hartmann V, Tlili A. Nickel-Catalyzed Amination of Aryl Carbamates with Ammonia European Journal of Organic Chemistry. 2017: 3496-3500. DOI: 10.1002/Ejoc.201700660 |
0.403 |
|
2017 |
Ghiazza C, Glenadel Q, Tlili A, Billard T. Trifluoromethylselenolation and Fluoroalkylselenolation of Alkenes by Electrophilic Addition European Journal of Organic Chemistry. 2017: 3812-3814. DOI: 10.1002/Ejoc.201700643 |
0.36 |
|
2017 |
Glenadel Q, Ghiazza C, Tlili A, Billard T. Copper-Catalyzed Direct Trifluoro- and Perfluoroalkylselenolations of Boronic Acids with a Shelf-Stable Family of Reagents Advanced Synthesis & Catalysis. 359: 3414-3420. DOI: 10.1002/Adsc.201700904 |
0.4 |
|
2016 |
Tlili A, Toulgoat F, Billard T. Synthetic Approaches to Trifluoromethoxy-Substituted Compounds. Angewandte Chemie (International Ed. in English). 55: 11726-35. PMID 27467551 DOI: 10.1002/Anie.201603697 |
0.319 |
|
2016 |
Tlili A, Alazet S, Glenadel Q, Billard T. Copper-Catalyzed Perfluoroalkylthiolation of Alkynes with Perfluoroalkanesulfenamides. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 10230-4. PMID 27334703 DOI: 10.1002/Chem.201601338 |
0.407 |
|
2016 |
Glenadel Q, Bordy M, Alazet S, Tlili A, Billard T. Metal-Free Direct Nucleophilic Perfluoroalkylthiolation with Perfluoroalkanesulfenamides Asian Journal of Organic Chemistry. 5: 428-433. DOI: 10.1002/Ajoc.201600003 |
0.387 |
|
2015 |
Chauvier C, Tlili A, Das Neves Gomes C, Thuéry P, Cantat T. Metal-free dehydrogenation of formic acid to H2 and CO2 using boron-based catalysts. Chemical Science. 6: 2938-2942. PMID 29308170 DOI: 10.1039/C5Sc00394F |
0.35 |
|
2015 |
Glenadel Q, Alazet S, Tlili A, Billard T. Mild and Soft Catalyzed Trifluoromethylthiolation of Boronic Acids: The Crucial Role of Water. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 14694-8. PMID 26271228 DOI: 10.1002/Chem.201502338 |
0.39 |
|
2014 |
Toummini D, Tlili A, Bergès J, Ouazzani F, Taillefer M. Copper-catalyzed arylation of nitrogen heterocycles from anilines under ligand-free conditions. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 14619-23. PMID 25284684 DOI: 10.1002/Chem.201404982 |
0.387 |
|
2014 |
Schranck J, Tlili A, Beller M. Functionalization of remote C-H bonds: expanding the frontier. Angewandte Chemie (International Ed. in English). 53: 9426-8. PMID 25066575 DOI: 10.1002/Anie.201405714 |
0.469 |
|
2014 |
Pospech J, Tlili A, Spannenberg A, Neumann H, Beller M. Regioselective ruthenium-catalyzed carbonylative direct arylation of five-membered and condensed heterocycles. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 3135-41. PMID 24519915 DOI: 10.1002/Chem.201304314 |
0.543 |
|
2014 |
Tlili A, Schranck J, Pospech J, Neumann H, Beller M. Ruthenium-catalyzed hydroaroylation of styrenes in water through directed C-H bond activation Chemcatchem. 6: 1562-1566. DOI: 10.1002/Cctc.201402031 |
0.472 |
|
2014 |
Schranck J, Tlili A, Beller M. Regioselektive katalytische Funktionalisierung von entfernten C-H-Bindungen Angewandte Chemie. 126: 9580-9582. DOI: 10.1002/Ange.201405714 |
0.422 |
|
2013 |
Schranck J, Tlili A, Alsabeh PG, Neumann H, Stradiotto M, Beller M. Palladium-catalysed carbonylative α-arylation of acetone and acetophenones to 1,3-diketones. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 12624-8. PMID 24175338 DOI: 10.1002/Chem.201302590 |
0.51 |
|
2013 |
Schranck J, Wu XF, Tlili A, Neumann H, Beller M. A novel double carbonylation reaction of aryl halides: selective synthesis of 5-arylfuranones. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 12959-64. PMID 24022987 DOI: 10.1002/Chem.201302092 |
0.591 |
|
2013 |
Schranck J, Tlili A, Beller M. More sustainable formation of C-N and C-C bonds for the synthesis of N-heterocycles. Angewandte Chemie (International Ed. in English). 52: 7642-4. PMID 23775609 DOI: 10.1002/Anie.201303015 |
0.505 |
|
2013 |
Tlili A, Billard T. Formation of C-SCF3 bonds through direct trifluoromethylthiolation. Angewandte Chemie (International Ed. in English). 52: 6818-9. PMID 23657900 DOI: 10.1002/Anie.201301438 |
0.351 |
|
2013 |
Tlili A, Schranck J, Pospech J, Neumann H, Beller M. Ruthenium-catalyzed carbonylative C-C coupling in water by directed C-H bond activation. Angewandte Chemie (International Ed. in English). 52: 6293-7. PMID 23629872 DOI: 10.1002/Anie.201301663 |
0.486 |
|
2013 |
Schranck J, Tlili A, Alsabeh PG, Neumann H, Stradiotto M, Beller M. Palladium-catalysed carbonylative α-arylation of acetone and acetophenones to 1,3-diketones Chemistry - a European Journal. 19: 12624-12628. DOI: 10.1002/chem.201302590 |
0.371 |
|
2013 |
Schranck J, Tlili A, Beller M. Nachhaltigere Bildung von C-N- und C-C-Bindungen zur Synthese von N-Heterocyclen Angewandte Chemie. 125: 7795-7797. DOI: 10.1002/Ange.201303015 |
0.421 |
|
2013 |
Tlili A, Billard T. Bildung von C-SCF3-Bindungen durch direkte Trifluormethylthiolierung Angewandte Chemie. 125: 6952-6954. DOI: 10.1002/Ange.201301438 |
0.306 |
|
2012 |
Tlili A, Schranck J, Neumann H, Beller M. Discrete iron complexes for the selective catalytic reduction of aromatic, aliphatic, and α,β-unsaturated aldehydes under water-gas shift conditions. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 15935-9. PMID 23143970 DOI: 10.1002/Chem.201203059 |
0.451 |
|
2012 |
Schranck J, Tlili A, Neumann H, Alsabeh PG, Stradiotto M, Beller M. A selective palladium-catalyzed carbonylative arylation of aryl ketones to give vinylbenzoate compounds. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 15592-7. PMID 23143936 DOI: 10.1002/Chem.201202895 |
0.517 |
|
2012 |
Danoun G, Tlili A, Monnier F, Taillefer M. Direct copper-catalyzed α-arylation of benzyl phenyl ketones with aryl iodides: route towards tamoxifen. Angewandte Chemie (International Ed. in English). 51: 12815-9. PMID 23143836 DOI: 10.1002/Anie.201206024 |
0.41 |
|
2012 |
Tlili A, Monnier F, Taillefer M. Selective one-pot synthesis of symmetrical and unsymmetrical di- and triarylamines with a ligandless copper catalytic system. Chemical Communications (Cambridge, England). PMID 22618353 DOI: 10.1039/C2Cc32252H |
0.412 |
|
2012 |
Lefèvre G, Franc G, Tlili A, Adamo C, Taillefer M, Ciofini I, Jutand A. Contribution to the mechanism of copper-catalyzed C-N and C-O bond formation Organometallics. 31: 7694-7707. DOI: 10.1021/Om300636F |
0.367 |
|
2010 |
Tlili A, Monnier F, Taillefer M. Selective one-pot access to symmetrical or unsymmetrical diaryl ethers by copper-catalyzed double arylation of a simple oxygen source. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 12299-302. PMID 20853289 DOI: 10.1002/Chem.201001373 |
0.359 |
|
2009 |
Tlili A, Xia N, Monnier F, Taillefer M. A very simple copper-catalyzed synthesis of phenols employing hydroxide salts. Angewandte Chemie (International Ed. in English). 48: 8725-8. PMID 19827073 DOI: 10.1002/Anie.200903639 |
0.399 |
|
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