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Dr. Olivier Baslé (CV) |
Olivier Baslé completed his Master degree under the supervision of Prof. P.H Dixneuf at the university of Rennes in 2005 and obtained his PhD degree in 2009 at McGill University under the guidance of Prof. C.-J. Li. After postdoctoral studies with Prof. J. Rodriguez and T. Constantieux in Marseille and Dr. D. Bourrisou in Toulouse, he was appointed Chargé de Recherche (CNRS) at Ecole Nationale Supérieure de Chimie de Rennes in 2011 (Mauduit Group). In 2018, he joined the CNRS Laboratory of Coordination Chemistry (LCC) in Toulouse. His research program focuses on the development of selective catalytic transformations using N-heterocyclic carbene-Metal complexes. His research interests include organic synthesis, organometallic chemistry and homogeneous catalysis.
RECENT PUBLICATIONS
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“Directed Ortho C-H Borylation catalyzed using Cp*Rh(III)-NHC Complexes.” J. Thongpaen, T. E. Schmid, L. Toupet, V. Dorcet, M. Mauduit, O. Baslé, Chem. Commun. 2018, 54, 8202-8205. |
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“A Versatile and Highly Z-Selective Olefin Metathesis Ruthenium Catalyst Based on a Readily Acessible N-Heterocyclic Carbene.” A. Dumas, R. Tarrieu, T. Vives, T. Roisnel, V. Dorcet, O. Baslé, M. Mauduit. ACS. Catal. 2018, 8, 3257-3262. |
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“Synthesis and Application of Stereoretentive Ruthenium Catalyst on the Basis of the M7 and the Ru-Benzylidene-Oxazinone Design.” A. Dumas, D. S. Müller, I. Curbet, L. Toupet, M. Rouen, O. Baslé, M. Mauduit. Organometallics 2018, 37, 829-834. |
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“Bleaching Earths as Powerful Additives for Ru-Catalyzed Self-Metathesis of Non-Refined Methyl Oleate at Pilot Scale.” J. Allard, I. Curbet, G. Chollet, F. Tripoteau, S. Sambou, F. Caijo, Y. Raoul, C. Crévisy, O. Baslé, M. Mauduit. Chem. Eur. J. 2017, 23,12729-12734. |
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“Readily Accessible Unsymmetrical Unsaturated 2,6-Diisopropylphenyl N-Heterocyclic Carbene Ligands. Applications in Enantioselective Catalysis.” R. Tarrieu, A. Dumas, J. Thongpaen, T. Vives, T. Roisnel, V. Dorcet, C. Crévisy, O. Baslé, M. Mauduit. J. Org. Chem. 2017, 82, 1880-1887. |
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“From Environmentally Reusable Ionic-Tagged Ruthenium-Based Complexes to Industrially Relevant Homogeneous Catalysts: Toward a Sustainable Olefin Metathesis.” T. E. Shmid, A. Dumas, S. Colombel-Rouen, C. Crévisy, O. Baslé, M. Mauduit. Synlett. 2017, 28, 773-798 (review) |
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“Selective Metathesis of α-Olefins from Bio-Sourced Fischer–Tropsch Feeds.” M. Rouen, P. Queval, E. Borré, L. Falivene, A. Poater, M. Berthod, F. Hugues, L. Cavallo, O. Baslé, H. Olivier-Bourbigou, M. Mauduit. ACS catal. 2016, 6, 7970-7976 |
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“Copper-Catalyzed Asymmetric Conjugate Addition of Dimethylzinc to Acyl-N-methylimidazole Michael Acceptors: Scope, Limitations and Iterative Reactions.” S. Drissi-Amraoui, T. E. Schmid, J. Lauberteaux, C. Crévisy, O. Baslé, R. Marcia de Figueiredo, S. Halbert, H. Gérard, M. Mauduit, J.-M. Campagne. Adv. Synth. Catal. 2016, 358, 2519-2540. |
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“Electronic and chiroptical properties of chiral cycloiridiated complexes bearing helicenic NHC ligands.” N. Hellou, C. Jahier-Diallo, O. Baslé, M. Srebro-Hooper, L. Toupet, T. Roisnel, E. Caytan, C. Roussel, N. Vanthuyne, J. Autschbach, M. Mauduit, J. Crassous. Chem. Commun. 2016, 52, 9243-9246. |
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“Copper-Catalyzed Asymmetric Conjugate Addition of Dimethylzinc to Acyl-N-methylimidazole Michael Acceptors : a Powerful Synthetic Platform.” S. Drissi-Amraoui, M. S. T. Morin, C. Crévisy, O. Baslé, R. Marcia de Figueiredo, M. Mauduit, J.-M. Campagne. Angew. Chem. Int. Ed. 2015, 54, 11830-11834. |
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“Latent Ruthenium-Indenylidene Catalyst bearing a N-Heterocyclic Carbene and a Bidentate Picolinate.” T. Shmid, F. Modicom, A. Dumas, E. Borré L. Toupet, O.Baslé, M. Mauduit, Belstein J. Org. Chem. 2015, 11, 1541-1546. |
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“Efficiency of Industrially Relevant Atropisomeric Diphosphines in Copper-Catalyzed 1,4-Asymmetric Conjugate Addition of Dialkylzincs to Cyclic or Acyclic Enones or Dienones” M. S. T. Morin, T. Vives, O. Baslé, C. Crévisy, V. Ratovelomanana-Vidal, M. Mauduit. Synthesis, 2015, 47, 2570-2577. |
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“Multicomponent Synthesis of Chiral Bidentate Unsymmetrical Unsaturated N- Heterocyclic Carbenes: Copper-Catalyzed Asymmetric C-C Bond Formation.” C. Jahier-Diallo, M. S. T. Morin, P. Queval, M. Rouen, I. Artur, P. Querard, L. Toupet, C. Crévisy, O. Baslé, M. Mauduit. Chem. Eur. J. 2015, 21, 993-997. |
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“Cationic Bis N-Heterocyclic Carbene Ruthenium Complex: Structure and Application as Latent Catalyst in Olefin Metathesis.” M. Rouen, P. Queval, L. Falivene, J. Allard, L. Toupet, C. Crévisy, F. Caijo, O. Baslé, L. Cavallo, M. Mauduit. Chem. Eur. J. 2014, 20, 13716-13721. | ![]() |
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“Multicomponent Synthesis of (a)chiral Unsymmetrical Unsaturated N-Heterocyclic Carbene (U2-NHC) Precursors; and Their Related Transition-Metal Complexes” P. Queval, C. Jahier, M. Rouen, I. Artur, J.-C. Legeay, L. Falivene, L. Toupet, C. Crévisy, L. Cavallo, O. Baslé, M. Mauduit. Angew. Chem. Int. Ed. 2013, 52, 14103-14107. |
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« Enantioselective 1,6-Conjugate Addition of Dialkylzinc Reagents to Acyclic Dienones Catalyzed by Cu-DiPPAM Complex. Extension to asymmetric sequential 1,6/1,4 Conjugate Addition. » M. Magrez-Chiquet, M. S. T. Morin, J. Wencel-Delord, S. Drissi Amraoui, O. Baslé, A. Alexakis, C. Crévisy, M. Mauduit. Chem. Eur. J., 2013, 19, 13663. (Synfacts 2014, 10, 0042). |
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« Synergic Effects Between N-Heterocyclic Carbene and Chelating-Benzylidene-Ether Ligands Towards the Initiation Step of Hoveyda-Grubbs Type Ru-Complexes. » D. J. Nelson, P. Queval, M. Rouen, M. Magrez, F. Caijo, E. Borré, I. Laurent, C. Crévisy, O. Baslé, M. Mauduit, J. M. Percy. ACS Catalysis, 2013, 3, 259-264 |
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“Screening of a Selection of Commercially Available Homogeneous Ru-Catalysts in Valuable Olefin Metathesis Transformations.” F. Caijo, F. Tripoteau, A. Bellec, C. Crévisy, O. Baslé, M. Mauduit, O. Briel. Catal. Sci. Technol., 2013, 3, 429-435 |
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“Bidentate Hydroxyalkyl-NHC Ligands for Copper-Catalyzed Asymmetric Allylic Substitution of Allyl Phosphates with Grignard Reagents.” M. Magrez, Y. Le Guen, O. Baslé, C. Crévisy, M. Mauduit, Chem. Eur. J., 2013, 19, 1199-1203. (Synfacts 2013, 4, 0427) |
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