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Marc Taillefer - Publications

Affiliations: 
Université de Montpellier / CNRS 
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48 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2025 Kumar T, Yang Y, Ben Hassine A, Mali D, Prajapat Y, Khandelwal P, Bouquin M, Taillefer M, Massicot F, Chevreux S, Behr JB, Maron L, Jaroschik F. Lanthanide-mediated Defluorinative Transformations of Trifluoromethylated Benzofulvenes: Access to Functionalized Difluoroalkenes and Mechanistic Insights. Chemistry, An Asian Journal. e202500071. PMID 40079505 DOI: 10.1002/asia.202500071  0.555
2024 Pagès L, Kurpik G, Mollfulleda R, Abdine RAA, Walczak A, Monnier F, Swart M, Stefankiewicz AR, Taillefer M. Copper-Catalysed Synthesis of (E)-Allylic Organophosphorus Derivatives: A Low Toxic, Mild, Economical, and Ligand-Free Method. Chemsuschem. e202401450. PMID 39207806 DOI: 10.1002/cssc.202401450  0.366
2024 Geniller L, Ben Kraim H, Clot E, Taillefer M, Jaroschik F, Prieto A. Metal-free decarboxylative allylation of oxime esters under light irradiation. Chemistry (Weinheim An Der Bergstrasse, Germany). e202401494. PMID 38785147 DOI: 10.1002/chem.202401494  0.397
2023 Geniller L, Taillefer M, Jaroschik F, Prieto A. Photocatalyzed Amination of Alkyl Halides to Access Primary Amines. The Journal of Organic Chemistry. 89: 656-664. PMID 38061988 DOI: 10.1021/acs.joc.3c02431  0.34
2023 Pagès L, Bouquin M, Jaroschik F, Monnier F, Taillefer M. Copper-Catalyzed Regio- and Stereoselective Hydrothiolation of Allenamides, Enamides, and Ynamides. The Journal of Organic Chemistry. 88: 1168-1176. PMID 36599034 DOI: 10.1021/acs.joc.2c02716  0.355
2021 Blieck R, Lemouzy S, van der Lee A, Taillefer M, Monnier F. Synergistic Copper/Enamine Catalysis for the Regio-, Stereo-, and Enantioselective Intermolecular α-Addition of Aldehydes to Allenamides. Organic Letters. PMID 34780198 DOI: 10.1021/acs.orglett.1c03477  0.323
2021 Pagès L, Lemouzy S, Taillefer M, Monnier F. Easy Access to Allylic Sulfones Through Transition-Metal-Free Hydrosulfonylation Of Allenes. The Journal of Organic Chemistry. 86: 15695-15701. PMID 34661402 DOI: 10.1021/acs.joc.1c01345  0.39
2021 Prieto A, Taillefer M. Visible-Light Decatungstate/Disulfide Dual Catalysis for the Hydro-Functionalization of Styrenes. Organic Letters. PMID 33534594 DOI: 10.1021/acs.orglett.1c00189  0.33
2021 Kumar T, Yang Y, Sghaier S, Zaid Y, Le Goff X, Rousset E, Massicot F, Harakat D, Martinez A, Taillefer M, Maron L, Behr JB, Jaroschik F. Tuning the regioselective functionalization of trifluoromethylated dienes via lanthanum-mediated single C-F bond activation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33433035 DOI: 10.1002/chem.202005239  0.538
2019 Blieck R, Taillefer M, Monnier F. Copper-Catalyzed Hydrocarboxylation of -Allenyl Derivatives. The Journal of Organic Chemistry. 84: 11247-11252. PMID 31373199 DOI: 10.1021/Acs.Joc.9B01510  0.492
2019 Liu Y, Bergès J, Zaid Y, Ouazzani Chahdi F, Van der Lee A, Harakat D, Clot E, Jaroschik F, Taillefer M. Aerobic and Ligand-free Manganese-Catalyzed Homocoupling of Arenes or Aryl Halides via in-situ Formation of Aryllithiums. The Journal of Organic Chemistry. PMID 30665303 DOI: 10.1021/Acs.Joc.8B02834  0.334
2019 Bahri J, Tanbouza N, Ollevier T, Taillefer M, Monnier F. Hydrogen bond-promoted metal-free hydroamination of alkynes Synlett. 30: 2086-2090. DOI: 10.1055/S-0039-1690988  0.365
2019 Blieck R, Perego L, Ciofini I, Grimaud L, Taillefer M, Monnier F. Copper-Catalysed Hydroamination of N-Allenylsulfonamides: The Key Role of Ancillary Coordinating Groups Synthesis. 51: 1225-1234. DOI: 10.1055/S-0037-1611673  0.446
2019 Abdine RAA, Kurpik G, Walczak A, Aeash SAA, Stefankiewicz AR, Monnier F, Taillefer M. Mild temperature amination of aryl iodides and aryl bromides with aqueous ammonia in the presence of CuBr and pyridyldiketone ligands Journal of Catalysis. 376: 119-122. DOI: 10.1016/J.Jcat.2019.06.020  0.422
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  0.385
2018 Kumar T, Ben Hassine A, Martinez A, Harakat D, Chevreux S, Massicot F, Taillefer M, Behr JB, Vasse JL, Jaroschik F. Application of Elemental Lanthanides in the Selective C-F Activation of Trifluoromethylated Benzofulvenes Providing Access to Various Difluoroalkenes. Journal of Visualized Experiments : Jove. PMID 30102265 DOI: 10.3791/57948  0.551
2018 Blieck R, Abed Ali Abdine R, Taillefer M, Monnier F. Regio- and Stereoselective Copper-Catalyzed Allylation of 1,3-Dicarbonyl Compounds with Terminal Allenes. Organic Letters. 20: 2232-2235. PMID 29600714 DOI: 10.1021/Acs.Orglett.8B00575  0.459
2017 Perego LA, Blieck R, Michel J, Ciofini I, Grimaud L, Taillefer M, Monnier F. Copper-Catalyzed Hydroamination of N -Allenylazoles: Access to Amino-Substituted N -Vinylazoles Advanced Synthesis & Catalysis. 359: 4388-4392. DOI: 10.1002/Adsc.201700965  0.458
2016 Blieck R, Bahri J, Taillefer M, Monnier F. Copper-Catalyzed Hydroamination of Terminal Allenes. Organic Letters. 18: 1482-5. PMID 26959973 DOI: 10.1021/acs.orglett.6b00452  0.376
2016 Monnier F, Taillefer M. From Ruthenium to Copper: A la carte Tools for the Synthesis of Molecules of Interest. Chimia. 70: 53-60. PMID 26931218 DOI: 10.2533/Chimia.2016.53  0.434
2016 Fabre I, Perego LA, Bergès J, Ciofini I, Grimaud L, Taillefer M. Antagonistic Effect of Acetates in C-N Bond Formation with In Situ Generated Diazonium Salts: A Combined Theoretical and Experimental Study European Journal of Organic Chemistry. 2016: 5887-5896. DOI: 10.1002/Ejoc.201600891  0.459
2015 Bahri J, Blieck R, Jamoussi B, Taillefer M, Monnier F. Hydroamination of terminal alkynes with secondary amines catalyzed by copper: regioselective access to amines. Chemical Communications (Cambridge, England). PMID 26077650 DOI: 10.1039/c5cc02677f  0.377
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  0.401
2014 Pichette Drapeau M, Ollevier T, Taillefer M. On the frontier between nucleophilic aromatic substitution and catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 5231-6. PMID 24737493 DOI: 10.1002/chem.201304164  0.318
2013 Toummini D, Ouazzani F, Taillefer M. Iron-catalyzed homocoupling of aryl halides and derivatives in the presence of alkyllithiums. Organic Letters. 15: 4690-3. PMID 24004324 DOI: 10.1021/ol401987s  0.358
2013 Racine E, Monnier F, Vors JP, Taillefer M. Direct N-cyclopropylation of secondary acyclic amides promoted by copper. Chemical Communications (Cambridge, England). 49: 7412-4. PMID 23863880 DOI: 10.1039/c3cc42575d  0.325
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  0.315
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  0.378
2011 Racine E, Monnier F, Vors JP, Taillefer M. A simple copper-catalyzed synthesis of tertiary acyclic amides. Organic Letters. 13: 2818-21. PMID 21548643 DOI: 10.1021/ol200750p  0.403
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  0.315
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  0.373
2009 Monnier F, Taillefer M. Catalytic C-C, C-N, and C-O Ullmann-type coupling reactions. Angewandte Chemie (International Ed. in English). 48: 6954-71. PMID 19681081 DOI: 10.1002/anie.200804497  0.357
2009 Kaddouri H, Vicente V, Ouali A, Ouazzani F, Taillefer M. Copper-catalyzed arylation of nucleophiles by using butadienylphosphines as ligands: mechanistic insight. Angewandte Chemie (International Ed. in English). 48: 333-6. PMID 19040232 DOI: 10.1002/anie.200800688  0.347
2009 Xia N, Taillefer M. A very simple copper-catalyzed synthesis of anilines by employing aqueous ammonia. Angewandte Chemie (International Ed. in English). 48: 337-9. PMID 18830943 DOI: 10.1002/anie.200802569  0.368
2008 Monnier F, Turtaut F, Duroure L, Taillefer M. Copper-catalyzed sonogashira-type reactions under mild palladium-free conditions. Organic Letters. 10: 3203-6. PMID 18588308 DOI: 10.1021/ol801025u  0.405
2008 Xia N, Taillefer M. Copper- or iron-catalyzed arylation of phenols from respectively aryl chlorides and aryl iodides. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 6037-9. PMID 18494009 DOI: 10.1002/chem.200800436  0.337
2008 Rahier NJ, Volle JN, Lacour MA, Taillefer M. Reactivity of Ph3PNLi towards PIII and PV electrophiles Tetrahedron. 64: 6645-6650. DOI: 10.1016/J.Tet.2008.05.019  0.367
2007 Taillefer M, Xia N, Ouali A. Efficient iron/copper co-catalyzed arylation of nitrogen nucleophiles. Angewandte Chemie (International Ed. in English). 46: 934-6. PMID 17186562 DOI: 10.1002/anie.200603173  0.311
2007 Taillefer M, Xia N, Ouali A. Cover Picture: Efficient Iron/Copper Co‐Catalyzed Arylation of Nitrogen Nucleophiles (Angew. Chem. Int. Ed. 6/2007) Angewandte Chemie. 46: 807-807. DOI: 10.1002/Anie.200790013  0.364
2007 Taillefer M, Xia N, Ouali A. Titelbild: Efficient Iron/Copper Co-Catalyzed Arylation of Nitrogen Nucleophiles (Angew. Chem. 6/2007) Angewandte Chemie. 119: 821-821. DOI: 10.1002/Ange.200790014  0.392
2006 Ouali A, Laurent R, Caminade AM, Majoral JP, Taillefer M. Enhanced catalytic properties of copper in O- and N-arylation and vinylation reactions, using phosphorus dendrimers as ligands. Journal of the American Chemical Society. 128: 15990-1. PMID 17165724 DOI: 10.1021/ja066505s  0.354
2006 Taillefer M, Rahier N, Hameau A, Volle JN. A new and convenient method for the synthesis of strong non-ionic bases. Chemical Communications (Cambridge, England). 3238-9. PMID 17028755 DOI: 10.1039/B603677E  0.321
2006 Taillefer M, Ouali A, Renard B, Spindler JF. Mild copper-catalyzed vinylation reactions of azoles and phenols with vinyl bromides. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 5301-13. PMID 16680787 DOI: 10.1002/chem.200501411  0.429
2005 Cristau HJ, Ouali A, Spindler JF, Taillefer M. Mild and efficient copper-catalyzed cyanation of aryl iodides and bromides. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 2483-92. PMID 15714537 DOI: 10.1002/chem.200400979  0.464
2004 Cristau HJ, Cellier PP, Spindler JF, Taillefer M. Highly efficient and mild copper-catalyzed N- and C-arylations with aryl bromides and iodides. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 5607-22. PMID 15457520 DOI: 10.1002/Chem.200400582  0.514
2004 Cristau HJ, Cellier PP, Hamada S, Spindler JF, Taillefer M. A general and mild Ullmann-type synthesis of diaryl ethers. Organic Letters. 6: 913-6. PMID 15012063 DOI: 10.1021/ol036290g  0.409
2004 Cristau H, Cellier PP, Spindler J, Taillefer M. Mild Conditions for Copper‐Catalysed N‐Arylation of Pyrazoles European Journal of Organic Chemistry. 2004: 695-709. DOI: 10.1002/Ejoc.200300709  0.463
2004 Cristau H, Cellier PP, Spindler J, Taillefer M. Cover Picture: Efficient and Mild Copper‐Catalyzed N‐ and C‐Arylations with Aryl Bromides and Iodides (Chem. Eur. J. 22/2004) Chemistry: a European Journal. 10: 5557-5557. DOI: 10.1002/Chem.200490074  0.377
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