Institut de Chimie Moléculaire et des Matériaux d'Orsay

Jerôme Hannedouche

Chargé de Recherche
Bât. 420LCM – ICMMO
Université Paris-Sud
15, rue Georges Clémenceau
91405 Orsay Cedex
FRANCE

+33 1 69 15 47 40
jerome.hannedouche@u-psud.fr

ORCIDResearcherIDResearchGate

Jérôme Hannedouche received his PhD degree (2004) from the University of Warwick (UK) under the supervision of Prof. Martin Wills. After a 2-year postdoctoral stay at the Université Catholique de Louvain (Belgium) with Prof. Olivier Riant, he was appointed (2006) at the Institut de Chimie Moléculaire et des Matériaux d’Orsay (ICMMO) (Université Paris-Sud/Université Paris-Saclay, France) as a CNRS fellow researcher. His research interests lie in the development and mechanistic study of novel synthetic methodologies in asymmetric catalysis, mainly for C–N bond formation via hydroamination reaction catalysed by rare-earth and first-row late transition metal elements.

Well-Defined β-Diketiminatocobalt(II) Complexes for Alkene Cyclohydroamination of Primary Amines. C. Lepori, P. Gómez-Orellana, A. Ouharzoune, R. Guillot, A. Lledós, G. Ujaque, J. Hannedouche, ACS Catalysis, 2018, 4446-4451.

Well-Defined Four-Coordinate Iron(II) Complexes For Intramolecular Hydroamination of Primary Aliphatic Alkenylamines. E. Bernoud, P. Oulié, R. Guillot, M. Mellah, J. Hannedouche, Angew. Chem. Int. Ed., 2014, 53, 4930-4934.

Anti-Markovnikov Hydroamination of Aromatic Alkenes with Secondary Amines Catalyzed by Easily Accessible Yttrium Complexes. S. Germain, E. Schulz, J. Hannedouche, ChemCatChem, 2014, 6, 2065-2073.

Asymmetric Assisted Tandem Catalysis: Hydroamination followed by Asymmetric Friedel–Crafts Reaction from a Single Chiral N,N,N′,N′-Tetradentate Pyridylmethylamine-Based Ligand. A. Aillerie, V. Rodriguez-Ruiz, R. Carlino, F. Bourdreux, R. Guillot, S. Bezzenine-Lafollée, R. Gil, D. Prim, J. Hannedouche, ChemCatChem, 2016, 8, 2455–2460 .

Simple Chiral Diaminobinaphthyl Dilithium Salts for Intramolecular Catalytic Asymmetric Hydroamination of Amino-1,3-dienes. J. Deschamp, C. Olier, E. Schulz, R. Guillot, J. Hannedouche, J. Collin, Adv. Synth. & Catal., 2010, 352, 2171-2176.

Convenient method for the rapid generation of highly active and enantioselective yttrium catalysts for asymmetric hydroamination. J. Hannedouche, I. Aillaud, J. Collin, E. Schulz, A. Trifonov, Chem. Commun., 2008, 3552-3554.

C1-symmetric β-Diketiminatoiron(II) Complexes for Hydroamination of Primary Alkenylamines. C. Lepori, R. Guillot, J. Hannedouche, Advanced Synthesis & Catalysis, 2018, 0

Experimental and computational mechanistic studies of the β-diketiminatoiron(II)-catalysed hydroamination of alkenes tethered to primary amines. C. Lepori, E. Bernoud, R. Guillot, S. Tobisch, J. Hannedouche, Chemistry – A European Journal, 2018

Hydroamination and Hydroaminoalkylation of Alkenes by Group 3–5 Elements: Recent Developments and Comparison with Late Transition Metals. J. Hannedouche, E. Schulz, Organometallics, 2018, 37, 4313-4326

Mechanistic Insights into First-row Late Transition Metal-catalysed (formal) Hydroamination of Unactivated Alkenes. J. Hannedouche, CHIMIA, 2018, 72, 635-641

Facile Preparation of Vinyl S-Trifluoromethyl NH Aryl Sulfoximines. A.-L. Barthelemy, A. Prieto, P. Diter, J. Hannedouche, M. Toffano, E. Anselmi, E. Magnier, Eur. J. Org. Chem., 2018, 3764-3770

Well-Defined β-Diketiminatocobalt(II) Complexes for Alkene Cyclohydroamination of Primary Amines. C. Lepori, P. Gómez-Orellana, A. Ouharzoune, R. Guillot, A. Lledós, G. Ujaque, J. Hannedouche, ACS Catal., 2018, 4446-4451

First-Row Late Transition Metals for Catalytic (Formal) Hydro­amination of Unactivated Alkenes. C. Lepori, J. Hannedouche, Synthesis, 2017, 49, 1158-1167

First-Row Late Transition Metals for Catalytic Alkene Hydrofunctionalisation: Recent Advances in C-N, C-O and C-P Bond Formation. S. Bezzenine-Lafollée, R. Gil, D. Prim, J. Hannedouche, Molecules, 2017, 22, 1901-1929

Lithium-Catalyzed anti-Markovnikov Intermolecular Hydroamination Reactions of Vinylarenes and Simple Secondary Amines. S. Germain, M. Lecoq, E. Schulz, J. Hannedouche, ChemCatChem, 2017, 9, 1749-1753

Novel yttrium and zirconium catalysts featuring reduced Ar-BIANH2 ligands for olefin hydroamination (Ar-BIANH2 = bis-arylaminoacenaphthylene). A. Cimino, F. Moscatelli, F. Ferretti, F. Ragaini, S. Germain, J. Hannedouche, E. Schulz, L. Luconi, A. Rossin, G. Giambastiani, New J. Chem., 2016, 40, 10285-10293

Asymmetric Assisted Tandem Catalysis: Hydroamination followed by Asymmetric Friedel–Crafts Reaction from a Single Chiral N,N,N′,N′-Tetradentate Pyridylmethylamine-Based Ligand. A. Aillerie, V. Rodriguez-Ruiz, R. Carlino, F. Bourdreux, R. Guillot, S. Bezzenine-Lafollée, R. Gil, D. Prim, J. Hannedouche, ChemCatChem, 2016, 8, 2455–2460

Mixing and matching chiral cobalt- and manganese-based calix-salen catalysts for the asymmetric hydrolytic ring opening of epoxides. H. Dandachi, E. Zaborova, E. Kolodziej, O. R.-P. David, J. Hannedouche, M. Mellah, N. Jaber, E. Schulz, Tetrahedron: Asymmetry, 2016, 27, 246-253

Recent advances in metal free- and late transition metal-catalysed hydroamination of unactivated alkenes. E. Bernoud, C. Lepori, M. Mellah, E. Schulz, J. Hannedouche, Catal. Sci. Technol., 2015, 5, 2017-2037

Recent developments in alkene hydro-functionalisation promoted by homogeneous catalysts based on earth abundant elements: formation of C-N, C-O and C-P bond. V. Rodriguez-Ruiz, R. Carlino, S. Bezzenine-Lafollee, R. Gil, D. Prim, E. Schulz, J. Hannedouche, Dalton Trans., 2015, 44, 12029-12059

Anti-Markovnikov Hydroamination of Aromatic Alkenes with Secondary Amines Catalyzed by Easily Accessible Yttrium Complexes. S. Germain, E. Schulz, J. Hannedouche, ChemCatChem, 2014, 6, 2065-2073

Well-Defined Four-Coordinate Iron(II) Complexes For Intramolecular Hydroamination of Primary Aliphatic Alkenylamines. E. Bernoud, P. Oulié, R. Guillot, M. Mellah, J. Hannedouche, Angewandte Chemie International Edition, 2014, 53, 4930-4934

Cationic Group-IV pincer-type complexes for polymerization and hydroamination catalysis. L. Luconi, J. Klosin, A. J. Smith, S. Germain, E. Schulz, J. Hannedouche, G. Giambastiani, Dalton Trans., 2013, 42, 16056-16065

Asymmetric Hydroamination: A Survey of the Most Recent Developments. J. Hannedouche, E. Schulz, Chemistry – A European Journal, 2013, 19, 4972-4985

Intramolecular Hydroamination Reactions Catalyzed by Neutral and Cationic Group IV Pyridylamido Complexes. L. Luconi, A. Rossin, G. Tuci, S. Germain, E. Schulz, J. Hannedouche, G. Giambastiani, ChemCatChem, 2013, 5, 1142-1151

LiCl-effect on asymmetric intramolecular hydroamination catalyzed by binaphthylamido yttrium complexes. Y. Chapurina, R. Guillot, D. Lyubov, A. Trifonov, J. Hannedouche, E. Schulz, Dalton Trans., 2013, 42, 507-520

29Si-1H IMPACT HMBC: a suitable tool for analyzing silylated derivatives. J. Farjon, A. Giros, S. Deloisy, L. Blanco, J. Hannedouche, E. Schulz, D. Merlet, Magnetic Resonance in Chemistry, 2013, 51, 230-233

Intramolecular enantioselective hydroamination catalyzed by rare earth binaphthylamides. J. Hannedouche, J. Collin, A. Trifonov, E. Schulz, J. Organomet. Chem., 2011, 696, 255-262

Alkyl Complexes of Lanthanum and Samarium Supported by a Chiral Binaphthylamido Ligand. Syntheses, Structures, and Catalytic Activity in Hydroamination of Amino-1,3-dienes. I. Aillaud, C. Olier, Y. Chapurina, J. Collin, E. Schulz, R. Guillot, J. Hannedouche, A. Trifonov, Organometallics, 2011, 30, 3378-3385

Catalytic, Enantioselective Intramolecular Hydroamination of Primary Amines Tethered to Di- and Trisubstituted Alkenes. Y. Chapurina, H. Ibrahim, R. Guillot, E. Kolodziej, J. Collin, A. Trifonov, E. Schulz, J. Hannedouche, J. Org. Chem., 2011, 76, 10163-10172

Comparison of yttrium binaphthylamido alkyl and amide complexes for enantioselective intramolecular hydroamination. I. Aillaud, J. Collin, J. Hannedouche, E. Schulz, A. Trifonov, Tetrahedron Lett., 2010, 51, 4742-4745

Well-defined and easily accessible yttrium complexes for enantioselective cyclisation of amines tethered to 1,2-di-substituted alkenes. Y. Chapurina, J. Hannedouche, J. Collin, R. Guillot, E. Schulz, A. Trifonov, Chem. Commun., 2010, 46, 6918-6920

Enantioselective Intramolecular Hydroamination of Secondary Amines Catalyzed by Easily Accessible Ate and Neutral Rare-Earth Complexes. C. Queffelec, F. Boeda, A. Pouilhès, A. Meddour, C. Kouklovsky, J. Hannedouche, J. Collin, E. Schulz, ChemCatChem, 2010, 3, 122-126

Simple Chiral Diaminobinaphthyl Dilithium Salts for Intramolecular Catalytic Asymmetric Hydroamination of Amino-1,3-dienes. J. Deschamp, C. Olier, E. Schulz, R. Guillot, J. Hannedouche, J. Collin, Adv. Synth. & Catal., 2010, 352, 2171-2176