Publications and Patents

2020_______________________________________________

  • V. Davenel, C. Nisole, F. Fontaine-Vive, J.-M. Fourquez, A.-M. Chollet, V. Michelet "Gold-Catalyzed Cycloisomerization of 1,6-Cyclohexenylalkyne: An Efficient Entry to Bicyclo[3.2.1]oct-2-ene and Bicyclo[3.3.1]nonadiene" J. Org. Chem. 2020, 85, 12657–12669.
  • V. Marsicano, A. Arcadi, M. Aschi, V. Michelet "Experimental and Computational Evidences on Gold-Catalyzed Regioselective Hydration of Phthalimido-Protected Propargylamines: An Entry to β-Amino Ketones" Org. Biomol. Chem. 2020, doi.org/10.1039/D0OB01598A.
  • C. F. Heinrich, D. Durand, J. Starck, V. Michelet "Ruthenium Metathesis: A Key Step To Access a New Cyclic Tetrasubstituted Olefin Platform" Org. Lett. 2020, 22, 7064-7067.
  • X. Chen, F. Fontaine-Vive, S. Poulain-Martini, V. Michelet Silver-catalyzed intramolecular [4 + 2] cycloaddition reaction of amide-1,6-enynes Catal. Commun. 2020,  doi.org/10.1016/j.catcom.2020.106117.
  • L. Seijo, P. Ondet, S. Olivero and E. Duñach "Heterogeneous catalysis for the tandem cyclisation of unsaturated alcohols" New J. Chem 2020, 44, 10479-10483.
  • R. Laher, C. Marin, V. Michelet "When Gold Meets Perfumes: Synthesis of Olfactive Compounds via Gold-Catalyzed Cycloisomerization Reactions" Org. Lett. 2020, 22, 4058-4062.
  • A. Omrania, F. Rezgui, E Dunach, S. Poulain-Martini "Bi(OTf)3-catalysed regioselective arylation of Morita-Baylis-Hillman type allylic electrophiles" Tetrahedron Letters 2020, 61, 151758-151762
  • A. Di Nicola, V. Marsicano, A. Arcadi, V. Michelet "Room temperature palladium-catalyzed hydroarylation of ynamides in water" Tetrahedron Letters 2020, 61, 151725-151729.
  • N. Boufroua, E. Dunach, F. Fontaine-Vive, S. Achouche-Bouzroura, S. Poulain-Martini "In(OTf)3-Catalysed Easy Access to Dihydropyranocoumarin and Dihydropyranochromone Derivatives" New J. Chem 2020, 44, 6042-6052.
  • R. K. Donato, A Mija, “Keratin associations with synthetic, biosynthetic and natural polymers: an extensive review”, Polymers, MDPI, 2020,12, 32; doi:10.3390/polym12010032.
  • C. Cantarutti, R. Dinu, A. Mija, “Biorefinery by-products and epoxy biorenewable monomers: a structural elucidation of humins and triglycidyl phloroglucinol crosslinking", Biomacromolecules, 2020, 21(2), 517-533
  • T-N. Tran, C. Di Mauro, A. Graillot, A. Mija, « Chemical reactivity and the influence of initiators on the epoxidized vegetable oil-dicarboxylic acid system”, Macromolecules,  2020, 53(7), 2526-2538.
  • C. Di Mauro, T-N. Tran, A. Graillot, A. Mija, « Enhancing the Reprocessing of a Vegetable Oil-Based Epoxy Thermoset by Initiator’s Nature Influence During Crosslinking and Recyclability”, ACS Sustain Chem, 2020, DOI:10.1021/acssuschemeng.0c01419
  • R. Dinu, C. Cantarutti, A. Mija, ”Design of sustainable materials by crosslinking a biobased epoxide with keratin and with lignin”, ACS Sustain Chem Eng, 2020, 10.1021/acssuschemeng.0c01759
  • P. Tosi, G. P. M. van Klink, C. Hurel, C. Lomenech, A. Celzard,V. Fierro, C. Delgado-Sanchez, A. Mija, “Investigating the properties of humins foams, the porous carbonaceous materials derived from biorefinery by-products”, Applied Materials Today, 2020, 20, 100622.
  • R. Dinu, A. Mija, " Bio-Based Composites from Industrial By-products and Wastes as Raw Materials”, J. Mater. Sci. Res., 2020, 9(2); doi:10.5539/jmsr.v9n1p29
  • C. Cantarutti, R. Dinu, A. Mija, “Polyhydroxybutyrate Bioresins with High Thermal Stability by Cross-linking with Resorcinol Diglycidyl Ether", Biomacromolecules, 2020, doi.org/10.1021/acs.biomac.0c00876, (invited cover page)
  • E. Licsandru, M. Gaysinski, A. Mija, “Structural Insights of Humins/Epoxidized Linseed Oil/ Hardener Terpolymerization”; Polymers, 2020, 12(7), 1583
  • T-N. Tran, C. Di Mauro, A. Graillot, A. Mija, « Monitoring the Structure-Reactivity Relationship on New Epoxidized Vegetable Oils Based Thermosetting Resins”, Polym Chem 2020, DOI: 10.1039/d0py00688b
  • C. Di Mauro, A. Genua,  A. Mija, “Building thermally and chemically reversible covalent bonds in vegetable oils based epoxy thermosets. Influence of epoxy-hardener ratio to promote recyclability”, Materials Advances, 2020, DOI: 10.1039/D0MA00370K
  • C. Di Mauro, S. Malburet, A. Genua, A. Graillot, A Mija, “Sustainable series of new epoxidized vegetable oils-based thermosets with chemical recycling properties”, Biomacromolecules 2020, DOI:10.1021/acs.biomac.0c01059
  • L. Chupin, L. Soccalingame, D. de Ridder, E. Gineau, G. Mouille, S. Arnoult, M. Brancourt-Hulmel, C. Lapierre, L. Vincent, A. Mija, S. Corn, N. Le Moigne, P. Navard, “Thermal and dynamic mechanical characterization of miscanthus stem fragments: effects of genotypes, internode levels and their relation with biochemical and structural characteristics”,  Industrial Crops and Products, 2020, 156,  https://doi.org/10.1016/j.indcrop.2020.112863
  • R. Dinu, A. Mija, “Sustainable Thermosets by Copolymerization of Humins with Triglycidyl Ether of Phloroglucinol”. Mater. Sci. Res., 2020, 9(2); doi: 10.5539/jmsr.v9n1p1.
  • C. Di Mauro, S. Malburet, A. Graillot, A Mija, Recyclable, Repairable and Reshapable (3R) ThermosetMaterials with Shape Memory Properties from Biobased Epoxidized Vegetable Oils, ACS Applied Bio Materials 2020, 10.1021/acsabm.0c01199

  • T.-N. Tran, C. Di Mauro, S. Malburet, A. Graillot, A. Mija, “Dual crosslinking of epoxidized linseed oil with combined aliphatic/aromatic diacids containing dynamic S-S bonds generating recyclable thermosets”, ACS Applied Bio Materials, 2020, 10.1021/acsabm.0c00788

  • A. Marotta, N. Faggio, V. Ambrogi, A. Mija, G. Gentile, P. Cerruti, “Bioderived furan-based epoxy/TiO2 nanocomposites for the preparation of coatings with improved chemical resistance”, Chem Eng J, 2021, 406, 127107, doi.org/10.1016/j.cej.2020.127107

2019_______________________________________________

  • A. Carrër, S. Turban, N. Provost, A. Caliez, G. Lamarche, G. Zanirato, M. Beucher, C. Pean, O. Mirguet, F. Perron-Sierra, V. Michelet. Juniperanol: First Total Synthesis and Evaluation in type 2 Diabetes Disease Bioorg. Chem. 2019, 92, 103243.
  • L. Lempenauer, G. Lemière, E. Duñach. Cyclisation Reactions Involving Alkyl Enol Ethers Adv. Synth. Catal. 2019, 361, 5284-5304.
  • X. Chen, S. Martini, V. Michelet A mild and regioselective synthesis of α-fluoroketones via gold and Selectfluor partnership Adv. Synth. Catal. 2019, 361, 3612-3618.
  • Y. Tang, I. Benaissa, M. Huynh, L. Vendier, N. Lugan, S. Bastin, P. Belmont, V. César, V. Michelet An Original L-shape, Tunable N-Heterocyclic Carbene Platform for Efficient Gold(I) Catalysis Angew. Chem. Int. Ed. 2019, 58, 7977-7981.
  • M. Laugeois, M. Vitale, V. Michelet, V. Ratovelomanana-Vidal The electron-poor vinylcyclopropanes in organometallic catalysis: interesting skeletons with various reactivities Iste OpenScience 2019, 19, 1-35. Published by ISTE Ltd. London, UK.
  • L. Lempenauer, A. Soupart, E. Duñach, G. Lemière. Synthesis and olfactory evaluation of allylic quaternary ether ketones, Flavour & Fragrance J., 2019, 34, 90-103.
  • L. Lempenauer, T. Appleson, G. Lemière, E. Duñach. Synthesis and olfactory evaluation of allylic quaternary thioether ketones, Flavour & Fragrance J., 2019, 34, 36-42.
  • A. Uehara, S. Olivero, B. Michelet, A. Martin-Mingot, S. Thibaudeau, E. Duñach. Direct and selective C-H carbamoylation of (hetero)aromatics with TMSOTf activated carbamoyl chloride, Eur. J. Org. Chem., 2019, 46-49.
  • D. Hector, S. Olivero, F. Orange, E. Duñach, J.-F. Gal, Quality control of a functionalized polymer catalyst by energy dispersive X-ray spectrometry (EDX/EDS), Anal. Chem., 2019, 91, 1773-1778.

  • E. M. Nuutinen, P. Willberg-Keyriläinen, T. Virtanen, A. Mija, L. Kuutti, R. Lantto, A.-S. Jaaskelainen, “Green process to regenerate keratin from feathers with an aqueous deep eutectic solvent”, RSC Advances, 9(34), 19720-19728, 2019

  • R. Dinu, A Mija, "Cross-linked polyfuran networks with elastomeric behaviour based on humins biorefinery by-products", Green Chemistry, 2019, 21, 6277 – 6289, (invited cover page)
  • X. Montane, R. Dinu, A Mija, “Synthesis of Resins Using Epoxies and Humins as Building Blocks: A Mechanistic Study Based on in situ FT-IR and NMR Spectroscopies", invited article on Molecules - "Macromolecular Chemistry" Section - Special Issue "Natural Polymers and Biopolymers II" 2019, doi:10.3390/molecules24224110
  • E. Licsandru, A Mija, “From biorefinery by-product to bioresins. Thermosets based on humins and epoxidized linseed oil”, Cellulose Chemistry & Technology, Advances in the Chemistry, Physics & Technology of Polysaccharides & Lignin, 53 (9-10), 963-969, 2019.
  • G. Falco, F. Giulieri, N. Volle, S. Pagnotta, N. Sbirrazzuoli, E. Peuvrel Disdier, A.Mija, »Self-organization of sepiolite fibbers in a biobased thermoset”, Composites Science and Technology 2019, 171, 226–233
  • A. Marotta, N. Faggio, V. Ambrogi, P. Cerruti, G. Gentile, A. Mija, « Curing Behavior and Properties of Sustainable Furan-Based Epoxy/Anhydride Resins”, Biomacromolecules, 2019, 20(10), 3831-3841
  • G. Falco, N. Sbirrazzuoli, A. Mija, »Biomass derived epoxy systems: From reactivity to final properties”, Materials Today Communications, 2019, 21, 100683.

2018_______________________________________________

  • Simion, A.; Candu, N.; Coman, S.M.; Primo, A.; Esteve-Adell, I.; Michelet, V.; Parvulescu, V.I.; Garcia, H. Bimetallic Oriented (Au/Cu2O) vs. Monometallic 1.1.1 Au (0) or 2.0.0 Cu2O Graphene-Supported Nanoplatelets as Very Efficient Catalysts for Michael and Henry Additions Eur. J. Org. Chem. 2018, 6185-6190. 
  • Rode, N. D.; Arcadi, A.; Di Nicola, A.; Marinelli, F.; Michelet, V. Gold-Catalyzed Cascade Reaction of β‑(2-Aminophenyl)-α,β-ynones with Ynamides: A Sequential Route to Polysubstituted 2‑Aminoquinolines Org. Lett. 2018, 20, 5103-5106.
  • Ye, F.; Tran, C.; Jullien, L.; Le Saux, T.; Haddad, M.; Michelet, V.; Ratovelomanana-Vidal, V. Synthesis of Fluorescent Azafluorenones and Derivatives via a Ruthenium-Catalyzed [2 + 2 + 2] Cycloaddition Org. Lett. 2018, 20, 4950-4953.
  • L. Lempenauer, A. Soupart, E. Duñach, G. Lemière. Synthesis of α-oxygenated β,γ-unsaturated ketones by a catalytic rearrangement strategy, Org. Biomol. Chem., 2018, 16, 5441-5445.
  • P. Ondet, G. Lemière, J. J. Filippi, E. Duñach. Stereocontrolled cascade cyclisation of campholenic enol-ether derivatives: en route to vetiver-scented spiroxides, Eur. J. Org. Chem, 2018, 980-989
  • Review: Toullec, P. Y.; Michelet, V. Gold-Catalyzed Polycyclization Toward Natural Products Synthesis Israel J. Chem. 2018, 578-585.
  • Grandclaudon, C.; Ruamps, M.; Duboc, R.; Michelet, V.; Toullec, P. Y. Assessing the Activity of Lewis Bases Organocatalysts in Halonium-Induced Carbocyclization Reactions Synlett 2018, 29, 1181-1186.
  • Ye, F.; Boukattaya, F.; Haddad, M.; Ratovelomanana-Vidal, V.; Michelet, V. Synthesis of 2-aminopyridines via rutheniumcatalyzed [2+2+2] cycloaddition of 1,6- and 1,7-diynes with cyanamides: scope and limitations New J. Chem. 2018, 42, 3222-3235.
  • Ye, F.; Haddad, M.; Ratovelomanana-Vidal, V.; Michelet, V. Rhodium-catalyzed asymmetric synthesis of 1,1-disubstituted 1,3-dihydrobenzo[c]furans from prochiral triynes and internal alkynes Catal. Commun. 2018, 107, 78-81.
  • Grandclaudon, C.; Michelet, V.; Toullec, P. Y. Iodonium-Induced Cyclization of N-Allenylindoles and N-Allenylpyrroles: An Access to Iododihydropyrido[1,2-a]indoles and Dihydroindolizines Synlett 2018, 29, 310-313.
  • Ling, J.; Laugeois, M.; Michelet, V.; Ratovelomanana-Vidal, V.; Vitale, M.R. Palladium(0)-Catalyzed Dearomatization of 2-Nitrobenzofurans through Formal (3+2) Cycloadditions with Vinylcyclopropanes: A Straightforward Access to Cyclopenta[b]benzofurans Synlett 2018, 29, 928-932.

2017_______________________________________________

  •  Ye, F.; Haddad, M.; Ratovelomanana-Vidal, V.; Michelet, V. Ruthenium-Catalyzed [2+2+2] Cycloaddition Reaction Forming 2-Aminopyridine Derivatives from α,ω-Diynes and Cyanamides Org. Lett. 2017, 19, 1104-1107.
  • Ye, F.; Haddad, M.; Michelet, V.; Ratovelomanana-Vidal, V. Solvent-Free Ruthenium Trichloride-Mediated [2+2+2] Cycloaddition of a,w-Diynes and Cyanamides: A Convenient Access to 2-Aminopyridines Org. Chem. Frontiers. 2017, 4, 1063-1068.
  • Laugeois, M.; Ling, J.; Férard, C.; Michelet, V.; Ratovelomanana-Vidal, V.; Vitale, M.R. Palladium(0)-Catalyzed Dearomative [3 + 2] Cycloaddition of 3-Nitroindoles with Vinylcyclopropanes: An Entry to Stereodefined 2,3-Fused Cyclopentannulated Indoline Derivatives Org. Lett. 2017, 19, 2266-2269.
  • Arcadi, A.; Chiarini, M.; Del Vecchio, L.; Marinelli, F.; Michelet, V. Sequential Silver-Catalyzed Oxidative Cyclization Reactions of Unprotected 2-Alkynylanilines to Anthranils. Eur. J. Org. Chem. 2017, 2214-2222. VIP article. Cover Picture
  • Tomas-Mendivil, E.; Heinrich, C.; Ortuno, J.-C.; Starck, J.; Michelet, V. Gold-catalyzed access to 1H-isochromenes: reaction development and mechanistic insight ACS Catal. 2017, 7, 380-387.
  • P. Ondet, C. Plessis, G. Lemière, E. Duñach, Synthesis and olfactory evaluation of spiro tricyclic diether structures, Flavour & Fragrance J., 2017, 32, 119-125. link
  •  P. Ondet, G. Lemière, E. Duñach, Cyclisations Catalysed by Bismuth(III) Triflate, Eur. J. Org. Chem., 2017, 761-780. link
  • G. Compain, L. Sick, L. Massi, E. Duñach, J. F. Gal, Bond Strength and Reactivity Scales for Lewis Superacid Adducts : A Comparative Study with In(OTf)3 and Al(OTf)3, ChemPhysChem., 2017, 18, 683-691. link
  • S. Olivero, E. Duñach, Electrosynthesis of boronic acids and esters, revue, Current Opinion in Electrochemistry, 2017, 2, 38-42. link
  • C. Iacobucci, N. Jouini, L. Massi, S. Olivero, G. F. De Angelis, E. Duñach, J.-F. Gal, Quantitative ligand affinity scales for metal triflate salts. Application to isomer differentiation, PlusPlusChem, 2017, 82, 498-506. link
  • M. J. Medeiros, S. Olivero, E. Duñach, Electrochemical cyclizations of organic halides catalyzed by electrogenerated nickel(I) complexes : towards environmentally friendly methodologies, revue, Electrochim. Acta, 2017, 373-381. link
  • V. Dalla, S. Antoniotti, E. Dunach, Atom Economical Catalytic Direct Substitution of N,O-Acetals with Simple Ketones, Eur. J. Org. Chem., 2017, 4445-4460. link
  • L. Lempenauer, E. Duñach, G. Lemière, Tuning the Reactivity of Functionalized Diallylic Alcohols : Brønsted Acid vs. Lewis Acid Catalysis, Chemistry, Eur. J., 2017, 23, 10285-10288. link

2016_______________________________________________

  • Ye, F.; Haddad, M.; Michelet, V.; Ratovelomanana-Vidal, V. Access toward Fluorenone Derivatives through Solvent-Free Ruthenium Trichloride Mediated [2 + 2 + 2] Cycloadditions Org. Lett. 2016, 18, 5612-5615.
  • Le Boucher d’Herouville, F.; Millet, A.; Scalone, M.; Michelet, V. Synthesis of Atropisomeric MeOBIPHEP Analogues and Their Application in Silver-Catalyzed Cycloisomerization of Allenols Synthesis 2016, 48, 3309-3316.
  • Bontemps, A.; Mariaule, G.; Desbène-Finck, S.; Helissey, P.; Giorgi-Renault, S.; Michelet, V.; Belmont, P. Silver-Catalyzed Domino Hydroarylation / Cycloisomerization Reactions on 2-alkynyl-3-carbaldehydequinolines: access to (hetero)aryl-pyranoquinolines Synthesis 2016, 48, 2178-2190.
  • Carrër, A.; Péan, C.; Perron-Sierra, F.; Mirguet, O.; Michelet, V. Gold-Catalyzed Cyclizations of Alkynyl Silyl Enol Ethers: an Easy Access to Bicyclo[3.2.1]octanone Derivatives Adv. Synth. Catal. 2016, 358, 1540-1545.
  • Laugeois, M.; Ponra, S.; Ratovelomanana-Vidal, V.; Michelet, V.; Vitale, M.R. Asymmetric preparation of polysubstituted cyclopentanes by synergistic Pd(0)/amine catalyzed formal [3+2] cycloadditions of vinyl cyclopropanes with enals Chem. Commun. 2016, 52, 5332-5335.
  • Grandclaudon, C.; Michelet, V.; Toullec, P. Y. Synthesis of Polysubstituted 2-Iodoindenes via Iodonium-Induced Cyclization of Arylallenes Org. Lett. 2016, 18, 676-679. Selected for Organic Chemistry Portal www.organic-chemistry.org/abstracts/lit5/300.shtm and www.organic-chemistry.org/synthesis/C1C/arenes/indenes.shtm
  • Arcadi, A.; Chiarini, M.; Del Vecchio, L.; Marinelli, F.; Michelet, V.  Silver- versus gold-catalyzed sequential oxidative cyclization of unprotected 2-alkynylanilines with oxone Chem. Commun. 2016, 52, 1458-1461.
  • Bell, J.; Samb, I.; Toullec, P. Y.; Michelet, V.; Leray I. Synthesis and complexing properties of molecular probes linked with fluorescent phosphane oxide derivatives J. Photochem. & Photobiol. A: Chem. 2016, 318, 25-32.
  • Ponra, S.; Vitale, M. R.; Michelet, V.; Ratovelomanana-Vidal, V. Practical synthesis of polysubstituted naphthalene derivatives via HNTf2-catalyzed benzannulation reaction Arkivoc 2016, ii, 62-81.
  • V. Morizur, D. Hector, S. Olivero, J. R. Desmurs, E. Duñach, Friedel-Crafts acylation with a polymer supported indium(III) catalyst, Synfacts, 2016, 10, 1105. link
  • B. Touati, A. El Bouakher, C. Taillier, R. Ben Othman, M. Trabelsi-Ayadi, S. Antoniotti, E. Duñach, V. Dalla, Enolizable Carbonyls and N,O-Acetals : A Rational Approach for Room-Temperature Lewis Superacid-Catalyzed Direct α-Amidoalkylation of Ketones and Aldehydes, Chem. Eur J. 2016, 22, 6012-6022. link
  • M. J. Neto, E. Duñach, J. M. S. S. Esperança, A. P. Esteves, M. J. Medeiros, M. M. Silva, Ionic Liquids for the Electroreductive Radical Cyclization of Unsaturated Bromo Derivatives Catalyzed by Nickel(II) complexes, J. Electrochem. Soc 2016, 163, G21-G25. link
  • L. Lempenauer, E. Duñach, G. Lemière, Catalytic rearrangement of 2-alkoxy diallyl alcohols : a straightforward access to polysubstituted cyclopentenones, Org. Lett., 2016, 18, 1326-1329. link
  • V. Morizur, D. Hector, S. Olivero, J. R. Desmurs, E. Duñach, Metal sulfonate polymers as catalysts for the heterogeneous acylation of aromatic derivatives, Eur. J. Org. Chem., 2016, 3126-3129. link
  • V. Morizur, M. Braglia, S. Olivero, J. R. Desmurs, P. Knauth, E. Duñach, New aromatic polymer electrolytes for application in lithium metal batteries, New J. Chem., 2016, 3126-3129. link
  • P. Ondet, L. Lempenauer, E. Duñach, G. Lemière, Bi(III) triflate catalysed tandem cyclisations towards complex polycyclic ethers, Org. Chem. Frontiers, 2016, 3, 999-1003. link
  • N. Sadou, S. Aichouche-Bouzroura, R. Nechak, B. Nedjar-Kolli, V. Morizur, S. Poulain-Martini, E. Dunach, Acid-Catalyzed Synthesis of Thiazolidin-4-ones, Polycyclic Aromatic Compounds, 2016, 1-11. link

2015_______________________________________________

  • Tomas-Mendivil, E.; Starck, J.; Ortuno, J.-C.; Michelet, V. Synthesis of Functionalized 1H-Isochromene Derivatives via a Au-Catalyzed Domino Cycloisomerization/Reduction Approach Org. Lett. 2015, 17, 6126-6129. Selected for Organic Chemistry Portal www.organic-chemistry.org/abstracts/lit5/230.shtm, www.organic-chemistry.org/chemicals/reductions/hantzsch-ester.shtm and http://www.organic-chemistry.org/synthesis/heterocycles/benzo-fused/isochromenes.shtm
  • Moragues, A.; Neatu, F.; Pârvulescu, V.I.; Marcos, M. D.; Amorós, P.; Michelet, V. Heterogeneous gold catalyst: synthesis, characterization and application in 1,4-addition of boronic acids to enones ACS Catal. 2015, 5, 5060-5067.
  • Leseurre, L; Le Boucher d’Herouville, F.; Millet, A.; Genêt, J.-P.; Scalone, M.; Michelet, V. Synthesis of atropisomeric chiral MeOBIPHEP analogues via Pd-catalyzed P-C coupling – Applications to asymmetric Rh-catalyzed C-C bond formations in water Catal. Commun. 2015, 69, 129-132.
  • Jacquet, J.; Auvinet, A.-L.; Mandadapu, A. K.; Haddad, M.; Ratovelomanana-Vidal, V.; Michelet, V. Practical Solvent-free RuCl3-Mediated Benzannulation Approach To Fused Functionalized Arenes Adv . Synth. Catal. 2015, 357, 1387-1392.
  • Book chapter: Genin, E.; Michelet, V. in Green Process Engineering – From Concepts to Industrial Applications Poux, M.; Cognet, P.; Gourdon, C. Eds, CRC Press Taylor & Francis Group, ISBN 9781482208177, Chapter 10: Water as solvent and solvent-free reactions
  • Book chapter: Michelet, V. Gold-catalyzed Domino Reactions Topics in Current Chemistry 2015, Homogeneous Gold Catalysis Ed: Slaughter, L. M.; 357, 95-132.
  • Ponra, S.; Vitale, M. R.; Michelet, V.; Ratovelomanana-Vidal, V. HNTf2‑Catalyzed Regioselective Preparation of Polysubstituted Naphthalene Derivatives Through Alkyne−Aldehyde Coupling J. Org. Chem. 2015, 80, 3250-3257.
  • Neaţu, F.; Ciobanu, M.; Stoflea, L. E.; Frunza, L.; Pârvulescu, V. I.; Michelet, V. Arylation of alkynes over hydrotalcite docked Rh-m-TPPTC complex Catalysis Today 2015, 247, 155-162.
  • Numéro spécial sur les récentes avancées en Chimie Organique et leurs applications potentielles dans l’industrie Vitale, M. R.; Lesuisse, D.; Michelet, V.; Ratovelomanana-Vidal, V. La catalyse duale synergique » Vers de nouvelles réactivités/sélectivités en synthèse organique Actualité Chimique 2015, 393-394, 74-81.
  • Michelet, V.; Scalone, M. (R)- and (S)-2,2'-Bis(diphenylphosphino)-6,6'-dimethoxy-1,1'-biphenyl Electronic Encyclopedia of Reagents for Organic Synthesis, Paquette L.; Fuchs, P.; Crich, D.; Wipf, P. Eds, John Wiley & Sons, 2015, 10.1002/047084289X.rn00832.pub2.
  • P. Tremel, C. Iacobucci, L. Massi, S. Olivero, J. F. Gal, E. Duñach, Catalytic carbonyl-ene reaction with ketones : evidence for a retro-ene process, New. J. Chem. 2015, 39, 7453-7458. link
  • V. Morizur, J. Szafranek, D. Bonhomme, S. Olivero, J. R. Desmurs, E. Duñach, Catalysis of the acylation of aromatic derivatives by metallic tosylates, Tetrahedron 2015, 71, 1752-1763. link
  • I. Diaf, A. Joffrin, G. Lemière, E. Dunach, Synthesis and odour evaluation of allenic derivatives, Flavour & Fragrance J. 2015, 478-484. link
  • S. Olivero, E. Duñach, Electrosynthèse d’acides et d’esters boroniques, L’Actualité Chimique 2015, 400-401, 29-30. link
  • Ondet, P. ; Joffrin, A. ; Diaf, I. ; Lemiere, G. ; Dunach, Cycloisomerization of Allene–Enol Ethers under Bi(OTf)3 Catalysis, E. Org. Lett. 2015, 17, 1002-1005. link
  • Clinet, A. ; Chaignaud, M. ; Clinet, J.-C. ; Duñach, E, Synthesis and odour evaluation of tricyclic ether derivatives containing a cis-1,2-dimethyl norbornane moiety, Flavour & Fragrance J. 2014, Flavour & Fragrance J. 2015, 30, 165-170. link
  • R. Nechak, S. Aichouche-Bouzroura, Y. Benmaleek, L. Salhi, S. Poulain-Martini, V. Morizur, E. Dunach, B. Nedjar-Kolli, Synthesis and antimicrobial evaluation of novel 4-thiazolodinones containing a pyrone moiety, Synth. Commun. 2015, 45, 262-272. link

 2014_______________________________________________

  • Book chapter: Genet, J.-P.; Toullec, P.Y.; Michelet, V. Carbophilic Cycloisomerization Reactions of Enynes and Domino Processes in Modern Alkyne Chemistry- Catalytic and Atom-Economic Transformations, B.M. Trost, C.-J. Li (Eds.), John Wiley & Sons; (2014), 3, ISBN: 978-3-527-33505-3, 27-68.
  • Mariaule, G.; Newsome, G.; Toullec, P. Y.; Belmont, P.; Michelet, V. Silver-Catalyzed Domino Hydroarylation/ Cycloisomerization Reactions of ortho-Alkynylbenzaldehydes: An Entry to Functionalized Isochromene Derivative Org. Lett. 2014, 16, 4570-4573.
  • Book chapter: Genin, E.; Michelet, V. Gold-catalyzed addition of HX on alkynes in The Chemistry of Organogold Compounds, 2014, Z. Rappoport, I. Marek, J. F. Liebman (Eds.), John Wiley & Sons; (2014), 10, 1-60, doi 10.1002/9780470682531.pat0814.
  • Praveen, C.; Levêque, S.; Vitale, M. R.; Michelet, V.; Ratovelomanana-Vidal, V. Synergistic Iron- and Amine-Catalysis in Carbocyclizations Synthesis 2014, 46, 1334-1338.
  • Pradal, A.; Gladiali, S.; Michelet, V.; Toullec, P. Y. Combinatorial Approach to Chiral Tris-ligated Carbophilic Platinum Complexes: Application to Asymmetric Catalysis Chem. Eur. J. 2014, 20, 7128-7135.
  • Bell, J.; Samb, I.; Toullec, P. Y.; Mongin, O. ; Blanchard-Desce, M.; Michelet, V.; Leray I. Ultra-Sensitive and Selective Hg2+ Chemosensors Derived from substituted 8-Hydroxyquinoline analogues New J. Chem. 2014, 38, 1072-1078.
  • Gold special issue, F.D. Toste Ed.: Arcadi, A.; Pietropaolo, E.; Alvino, A.; Michelet, V. Aminofluorination of 2-alkynylanilines: a Au-catalyzed entry to fluorinated indoles Beilstein J. Org. Chem. 2014, 10, 449-458.
  • Book chapter: Michelet, V. Noble Metal-Catalyzed Enyne Cycloisomerizations and Related Reaction in Comprehensive Organic Synthesis 2nd Edition, 2014, Ed. Molander, G.; Knochel, P., 1483-1536.
  • Book chapter: Toullec, P.Y.; Pradal, A.; Michelet, V. Asymmetric Gold-Catalyzed Reactions in Gold Catalysis: An Homogeneous Approach, 2014, Ed. Toste, F. D.; Michelet, V., Imperial College Press ; ISBN 978-1-84816-852-7 12, 445-500.
  • Morizur, V. ; Olivero, S. ; Desmurs, J. R. ; Knauth, P. ; Duñach, E., Novel lithium and sodium salts of sulfonamides and bis(sulfonyl)imides : synthesis and electrical conductivity, New J. Chem. 2014, 38, 6193-6197. link
  • Cacciuttolo, B. ; Poulain-Martini, S. ; Fontane-Vive, F. ; Hussein Abdou, M. A. ; El Kashef, H. ; Duñach, E., Access to polycyclic derivatives via triflate-catalyzed intramolecular hydroarylation, Eur J. Org. Chem. 2014, 7458-7468.link
  • Dunach, E., Carbon-carbon bond formation by Lewis superacid catalysis, Chemistry & Biodiversity 2014, 11, 1752-1763. link
  • Cacciuttolo, B. ; Ondet, P. ; Poulain-Martini, S. ; Lemiere, G. ; Dunach, E., Bi(III)-catalysed synthesis of substituted indanes by a double hydroarylation of unactivated 1,3-dienes, Org. Chem. Frontiers 2014, 1, 765-769. link
  • Labre, F. ; Gimbert, Y. ; Bannwarth, P. ; Olivero, S. ; Duñach, E. ; Chavant, P-Y., Application of cooperative iron/copper catalysis to a palladium-free borylation of aryl bromides with pinacolborane, Org. Lett. 2014, 16, 2366-2369. link
  • Dunach, E. ; Medeiros, M. J. ; Olivero, S., Electrochemical catalytic cyclization reactions using environmentally friendly methodologies, Renewable Energy Global Innovations Series 2014, ISSN 2291-2460.
  • Delattre, E. ; Lemière, G. ; Boulay, B. ; Desmurs, J.R. ; Dunach, E., Poly(vinyl alcohol) Functionalization with Aldehydes in Organic Solvents : Shining Properties of Poly(vinyl acetals), J. Appl. Polym. Sci. 2014, 131, 40677. link
  • Diaf, I. ; Lemière, G. ; Dunach, E., Metal Triflate-Catalysed Synthesis of Polycyclic Tertiary Alcohols by Cyclisation of gamma-Allenic Ketones, Angew. Chem., Int. Ed. 2014 , 53, 4177-4180. link
  • Nava, P. ; Carissian, Y. ; Drujon, J. ; Grau, F. ; Godeau, J. ; Antoniotti, S. ; Duñach, E. ; Humbel, S., Mechanistic insights into the 1,6-diene cycloisomerization catalyzed by Sn(NTf2)4, ChemCatChem 2014, 2, 663-672. link
  • Godeau, J. ; Grau, F. ; Antoniotti, S. ; Duñach, E., Preparation and olfactory evaluation of mono- and bicyclic compounds featuring gem-dimethylcyclohexane structures, Flavour & Fragrance J. 2014, 29, 59-66. link

2013_______________________________________________

  • Tomas-Mendivil, E.; Toullec, P.Y.; Borge, J.; Conejero, S.; Michelet, V.; Cadierno, V. New Water-Soluble Gold(I) and Gold(III) Complexes with Sulfonated NHC Ligands: Synthesis, Characterization and Application in the Catalytic Cycloisomerization of γ-Alkynoic Acids into Enol-Lactones ACS Catal. 2013, 3, 3086-3098.
  • Arcadi, A.; Pietropaolo, E.; Alvino, A.; Michelet, V. One-Pot Gold-Catalyzed Aminofluorination of Unprotected 2‑Alkynylaniline Org. Lett. 2013, 15, 2766-2769.
  • Auvinet, A.-L.; Michelet, V.; Ratovelomanana-Vidal, V. Solvent-free iridium(III)-catalyzed [2+2+2] cycloaddition. Access to fused arenes: isoindolines, dihydroisobenzofurans and indanes Synthesis 2013, 45, 2003-2008.
  • Auvinet, A.-L.; Ez-zoubir, M.; Bompard, S.; Vitale, M. R.; Brown, J. A.; Michelet, V.; Ratovelomanana-Vidal, V. Iridium(III)-Catalyzed Approach for the Synthesis of Fused Arenes: Access to Isoindolines, Indanes, and Dihydroisobenzofuran ChemCatChem 2013, 5, 2389-2394.
  • Praveen, C.; Montaignac, B.; Vitale, M. R.; Ratovelomanana-Vidal, V.; Michelet, V. Enantioselective Merger of Aminocatalysis with p-Lewis Acid Metal Catalysis: Asymmetric Preparation of Carbo- and Heterocycle ChemCatChem 2013, 5, 2395-2404.
  • Dunach, E. ; Medeiros, M. J. ; Olivero, S., Electrochemical catalytic cyclization reactions using environmentally friendly methodologies, J. Electrochem. Soc., 2013, 160, 3112-3116. link
  • Dunach, E., Catàlisi de la funcionalitzacio d’oléfines per superàcids de Lewis, Societat Catalana de Quimica 2013, 12, 50-54. ISSN : 2013-9853.
  • Romane, A. ; Belaqziz, R. ; Bahri, F. ; Fernandez, X. ; Antoniotti, S. ; Duñach, E., Essential oil composition and antibacterial activity of the different parts of Thymus maroccanus Ball : An Endemic Species in Morocco. Natural Product Research, 2013, 27, 1700-1704. link
  • Duñach, E. ; Medeiros, M.J. ; Olivero, S., Indirect Electrochemical Cyclization of Bromoalkoxylated Derivatives using Environmentally Friendly Methodologies, ECS Transactions, 2013, 45, 9-13. link
  • Constantieux, T. ; Duñach, E., Catalyse et synthèse asymétrique, L’Actualité Chimique, 2013, 377, 14-17. link
  • Salhi, L. ; Bouzroura-Aichouche, S. ; Benmaleek, Y. ;Bentarzi, Y. ; Poulain-Martini, S. ; Cacciuttolo, B. ; Dunach, E. ; Nedjar-Kolli, B., An efficient conversion of maleimide derivatives to 2-thioxo imidazolidinones, Org. Commun. 2013, 6, 87-94. link
  • Lemière, G. ; Dunach, E., Catalytic Activation of Olefins by Metal Triflates and Triflimides : Application to Fragrance Chemistry, Chem. Eur. J. 2013, 19, 3270-3280. link
  • Gal, J. F. ; Iacobucci, C. ; Monfardini, I. ; Massi, L. ; Duñach, E. ; Olivero, S., Metal triflates and triflimides as Lewis superacids : preparation, synthetic application and affinity tests by mass spectrometry, (Mini-review), J. Phys. Org. Chem., 2013, 26, 87-97. link
  • Clinet, A. ; Chaignaud, M. ; Clinet, J.-C. ; Dunach, E., Synthesis and odour evaluation of alcohols bearing a cis-1,2-dimethyl norbornane moiety, Flavour Fragrance J. 2013, 28, 53-61 link

2012_______________________________________________

  • Auvinet, A.-L.; Ez-zoubir, M.; Vitale, M. R.; Brown, J. A.; Michelet, V.; Ratovelomanana-Vidal, V. Practical and Efficient Iridium Catalyst for Benzannulation– An Entry To Isoindolines ChemSusChem 2012, 5, 1888-1891.
  • Pradal, A.; Faudot dit Bel, P.; Toullec, P. Y.; Michelet, V. Gold-Catalyzed C-H Oxidative Polyacyloxylation Reaction of Hindered Arenes Synthesis 2012, 44, 2463-2468.
  • Montaignac, B.; Praveen, C.; Vitale, M. R.; Michelet, V.; Ratovelomanana-Vidal, V. Enantioselective Metallo-Organocatalyzed Preparation of Cyclopentanes Bearing an All-Carbon Quaternary Stereocenter Chem. Commun. 2012, 48, 6559-6561.
  • Tomas-Mendivil, E.; Toullec, P.Y.; Diez, J.; Conejero, S.; Michelet, V.; Cadierno, V. Cycloisomerization versus Hydration Reactions in Aqueous Media: A Au(III)- NHC Catalyst That Makes the Difference Org. Lett. 2012, 14, 2520-2523.
  • Montaignac, B.; Östlund, V.; Vitale, M. R.; Ratovelomanana-Vidal, V.; Michelet, V. Copper(I)-Amine Metallo-Organocatalyzed Synthesis of Carbo- and Heterocyclic Systems  Org. Biomol. Chem. 2012, 10, 2300-2306. Top ten accessed articles for February 2012
  • Book chapter: Michelet, V.; Ratovelomanana-Vidal, V.; Pârvulescu, V.I.; Kočevar, M. Recent Advances in the Synthesis and Catalytic Hydrogenation of Dehydroamino Acid Derivatives and Bicyclo[2.2.2]octenes in Innovative Catalysis in Organic Synthesis - Oxidations, Hydrogenations, and C-X Bond Forming Reactions Anderson, P. Ed; Wiley-VCH, 2012, 131-152.
  • Gold cluster issue, F.D. Toste Ed.: Pradal, A.; Chen, Q.; Faudot dit Bel, P.; Toullec, P.Y.; Michelet, V. Gold-Catalyzed Cycloisomerization of Functionalized 1,5-Enynes – An Entry to Polycyclic Framework Synlett. 2012, 23, 74-79.
  • Godeau, J. ; Fontaine-Vive, F. ; Antoniotti, S. ; Dunach, E., Experimental and Theoretical Studies on the Bismuth-Triflate-Catalysed Cycloisomerisation of 1,6,10-Trienes and Aryl Polyenes, Chem. Eur. J. 2012, 18, 16815-16822 link
  • Lemiere, G. ; Cacciuttolo, B. ; Belhassen, E. ; Dunach, E., Bi(OTf)3-Catalyzed Cycloisomerization of Aryl-Allenes, Org. Lett. 2012, 14 , 2750-2753 link
  • Ben-David, M. ; Elias, M. ; Filippi, J. J. ; Dunach, E. ; Silman, I. ; Sussman, J. L. ; Tawfik, D.S., Catalytic versatility and backups in enzyme active sites : The case of serum paraoxonase 1, J. Molec Bio., 2012, 418, 181-196 link
  • Vece, V. ; Ben, H. H. K. ; Antoniotti, S. ; Dunach, E., C-O and C-C bond formation in the cyclisation of gem-(dialkoxymethyl)-1,6-dienes catalysed by tin(IV) triflimidate at room temperature, Tetrahedron Lett. 2012, 53 , 5102-5105 link
  • Legrave, N. ; Couhert, A. ; Olivero, S. ; Desmurs, J.-R. ; Dunach, E., Efficient Preparation of Anhydrous Metallic Triflates and Triflimides under Ultrasonic Activation, Eur. J. Org. Chem. 2012, 901-904 link
  • Gal, J.-F. ; Iacobucci, C. ; Monfardini, I. ; Massi, L. ; Dunach, E. ; Olivero, S., A Quantitative Approach of the Interaction between Metal Triflates and Organic Ligands Using Electrospray Mass Spectrometry, J. Am. Mass. Spec. 2012, 23, 2059-2062 link

2011_______________________________________________

  • Leseurre, L.; Püntener, K.; Genêt, J.-P.; Scalone, M.; Michelet, V. Synthesis of New Water-Soluble Atropisomeric Ligands Derived from the MeOBIPHEP Skeleton: Applications for Asymmetric CH Bond Formation and Mechanistic Studies  Adv. Synth. Catal. 2011, 353, 3269-3277.
  • Pradal, A.; Toullec, P.Y.; Michelet, V. Gold-Catalyzed Oxidative Acyloxylation of Arenes Org. Lett. 2011, 13, 6086-6089. Selected for Synform 2012, 3, A26 (M. Zanda) and Selected for Organic Chemistry Portal www.organic-chemistry.org/Highlights/2012/25June.shtm
  • Gold special issue, F.D. Toste Ed.: Pradal, A.; Chao, C.-M.; Toullec, P. Y.; Michelet, V. Asymmetric Au-catalyzed cycloisomerization of 1,6-enynes: An entry to bicyclo[4.1.0]heptene  Beilstein J. Org. Chem. 2011, 7, 1021-1029.
  • Le Boucher d’Herouville, F.; Millet, A.; Scalone, M.; Michelet, V. Room Temperature Rh-catalyzed Asymmetric 1,4-Addition of Arylboronic Acids to Maleimides and Enones in the Presence of CF3-Substituted MeOBIPHEP Analogues J. Org. Chem. 2011, 76, 6925-6930.
  • Leseurre, L.; Le Boucher d’Herouville, F.; Püntener, K.; Scalone, M.; Genêt, J.-P.; Michelet, V. Efficient Route to Atropisomeric Ligands Application to the Synthesis of MeOBIPHEP Analogues  Org. Lett. 2011, 13, 3250-3253.
  • Special issue Women in science: Montaignac, B.; Vitale, M. R.; Ratovelomanana-Vidal, V.; Michelet, V. Cooperative Copper(I) and Primary Amine Catalyzed Room Temperature Carbocyclization of Formyl Alkyne Eur. J. Org. Chem. 2011, 3723-3727.
  • Review: Pradal, A.; Toullec, P. Y.; Michelet, V. Recent Developments in Asymmetric Catalysis in the Presence of Chiral Gold Complexes Synthesis 2011, 1501-1514.
  • Pradal, A.; Chao, C.-M.; Vitale, M.; Toullec, P. Y.; Michelet, V. Asymmetric Au-Catalyzed Domino Cyclization / Nucleophile Addition Reactions of Enynes in the Presence of Water, Methanol and Electron-Rich Aromatic Derivatives Tetrahedron 2011, 67, 4371-4377.
  • Pradal, A.; Toullec, P. Y.; Michelet, V. Asymmetric Pt- and Au-cycloisomerization reactions of 1,n-enynes - Novel activities and new opportunities Chem. Today 2011, 29, 40-42.
  • Samb, I.; Bell, J.; Toullec, P. Y.; Michelet, V.; Leray I. Fluorescent Phosphane Selenide as Efficient Mercury Chemodosimeter  Org. Lett. 2011, 13, 1182-1185.
  • Alain-Rizzo, V.; Drouin-Kucma, D.; Rouxel, C.; Samb, I.; Bell, J.; Toullec, P. Y.; Michelet, V.; Leray I.; Blanchard-Desce, M. Synthesis, photophysical and two-photon absorption properties of elongated phosphane oxide and phosphane sulfide derivatives Chem. Asian. J. 2011, 6, 1080-1091.
  • Book chapter: Toullec, P. Y.; Michelet, V. Cycloisomerization of 1,n-enynes via carbophilic activation Topics in Current Chemistry 2011, Mechanisms of Transition Metal Catalyzed Transformations of Unsaturated Precursors: A Computational Approach Eds: Soriano, E.; Marco-Contelles, J.; 302, 31-80.
  • Gladiali, S.; Toullec, P. Y.; Genêt, J.-P.; Michelet, V. 4,5-Dihydro-4-phenyl-3H-dinaphto[2,1-c:1’,2’-e]phosphepin in Electronic Encyclopedia of Reagents for Organic Synthesis, Paquette L.; Fuchs, P.; Crich, D.; Wipf, P. Eds, John Wiley & Sons, 2011. doi 10.1002/047084289X.rn01271
  • Ez-Zoubir, M.; Brown, J.; Ratovelomanana-Vidal, V.; Michelet, V. Iridium-catalyzed hydroiodination of functionalized alkynes J. Organomet. Chem. 2011, 696, 433-441.
  • Godeau, J. ; Olivero, S. ; Antoniotti, S. ; Dunach, E., Biomimetic Cationic Polyannulation Reaction Catalyzed by Bi(OTf)3 : Cyclization of 1,6-Dienes, 1,6,10-Trienes, and Aryl Polyenes, Org. Lett. 2011, 13, 3320-3323 link
  • Cacciuttolo, B. ; Poulain-Martini, S. ; Dunach, E., Efficient Intramolecular Hydroarylation Catalysed by Bi(III) Triflate, Eur. J. Org. Chem. 2011, 3710-3714 link

2010_______________________________________________

  • Neaţu, F.; Protesescu, L.; Florea, M.; Pârvulescu, V. I.; Teodorescu, C. M.; Apostol, N.; Toullec, P. Y.; Michelet, V. Novel Pd heterogeneous catalysts for cycloisomerisation of acetylenic carboxylic acids Green Chem.2010, 12, 2145-2149.
  • Montaignac, B.; Vitale, M. R.; Ratovelomanana-Vidal, V.; Michelet, V. InCl3/CyNH2 Cocatalyzed Carbocyclization Reaction: An Entry to a-Disubstituted exo-Methylene Cyclopentane J. Org. Chem. 2010, 75, 8322-8325.
  • Pradal, A.; Nasr, A.; Toullec, P. Y.; Michelet, V. Room-Temperature Metal-Free Electrophilic 5-endo-Selective Iodocarbo-cyclization of 1,5-Enyne Org. Lett.2010, 12, 5222-5225. Selected in Synfacts as Synfact of the month 2011, 2, 163 (Contributors: M. Lautens and D. A. Candito)
  • Andreiadis, E.; Vitale, M. R.; Mézailles, N.; Le Goff, X.; Le Floch, P.; Toullec, P. Y.; Michelet, V. Chiral undecagold clusters: synthesis, characterization and investigation in catalysis Dalton Trans2010, 39, 10608-10616.
  • Ez-Zoubir, M.; Le Boucher d’Herouville, F.; Brown, J.; Ratovelomanana-Vidal, V.; Michelet, V. Stereoselective Ir(III)-Catalyzed Dimerization Reaction of Enynes: an Entry to Functionalized Polyunsaturated and Cyclic Systems Chem. Commun. 2010, 46, 6332-6334
  • Montaignac, B.; Vitale, M. R.; Michelet, V.; Ratovelomana-Vidal, V. Combined InCl3- and Amine-Catalyzed Intramolecular Addition of a-Disubstituted Aldehydes onto Unactivated Alkynes Org. Lett.2010, 12, 2582-2585. Selected for Organic Chemistry Portal www.organic-chemistry.org/abstracts/lit2/927.shtm and www.organic-chemistry.org/synthesis/C1C/cyclic/alkanes/cyclopentanes.shtm
  • Book chapter: Leseurre, L.; Genêt, J.-P.; Michelet, V. Coupling Reactions in Water in Handbook of Green Chemistry Series:Water as a Green Solvent P. Anastas, C.-J. Li Eds; John Wiley & Sons, 2010
  • Review: Toullec, P. Y.; Michelet, V. Chiral Cationic Platinum Complexes: New Catalysts For The Activation of Carbon-Carbon Multiple Bonds Towards Nucleophilic Enantioselective Attack Curr. Org. Chem.2010, 14, 1245-1253.
  • Numéro spécial « chimie et développement durable » – L’engagement des écoles de la Fédération Gay-Lussac Campagne, J.-M.; Agbossou, F.; Ayad, T.; Baudoin, O.; Buono, G.; Chataigner, I.; Crévisy, C.; Dez, I.; Donnard, M.; Fache, F.; Feasson, C.; Gaumont, A.-C.; Laurent Giordano, L.;  Peter Hesemann, P.; Marsais, F.; Mauduit, M.; Michelet, V.; Mortreux, A.; Phansavath, P.; Piva, O.; Roblin, J.-P.; Rouden, J.; Taillefer, M.; Toullec, P. Y.; Tschamber, T.; Vidal, V. Vers une chimie moléculaire verte Actualité Chimique 2010, 338-339, 14-27.
  • Ha-Thi, M.-H.; Delaire, J. A.; Michelet, V.; Leray, I. Sensitized Emission of Luminescent Lanthanide Complexes Based on a Phosphane Oxide Derivative J. Phys. Chem. A 2010, 114, 3264-3269.
  • Book chapter: Genin, E.; Leseurre, L.; Michelet, V. L’eau comme solvant et réactions sans solvant in Génie des procédés durables: du concept à la concrétisation industrielle; Poux, M.; Cognet, P.; Gourdon, C. Eds, Dunod, 2010 ISBN 978-2-10-055601-4, Chapter 10, 276-305. Prix Roberval de l’Enseignement Supérieur 2011
  • Vece, V. ; Ricci, J. ; Poulain-Martini, S. ; Nava, P. ; Carissan, Y. ; Humbel, S. ; Dunach, E., In(III)-Catalysed Tandem C-C and C-O Bond Formation between Phenols and Allylic Acetates, Eur. J. Org. Chem. 2010, , 6239-6248 link
  • Pintaric, C. ; Olivero, S. ; Gimbert, Y. ; Chavant, P. Y. ; Dunach, E., An Opportunity for Mg-Catalyzed Grignard-Type Reactions : Direct Coupling of Benzylic Halides with Pinacolborane with 10 mol% of Magnesium, J. Am. Chem. Soc. 2010, 132, 11825-11827 link
  • Muratore, A. ; Clinet, J.-C. ; Dunach, E., Synthesis of New exo- and endo-3,8-Dihydro-β-santalols and Other Norbornyl-Derived Alcohols, Chem. Biodiversity 2010, 7, 623-638 link
  • Monfardini, I. ; Massi, L. ; Tremel, P. ; Hauville, A. ; Olivero, S. ; Dunach, E. ; Gal, J.-F., Mass spectrometric characterization of metal triflates and triflimides (Lewis superacid catalysts) by electrospray ionization and tandem mass spectrometry, Rapid Commun. Mass Spectrom. 2010, 24 , 2611-2619 link
  • Monfardini, I. ; Massi, L. ; Dunach, E. ; Olivero, S. ; Gal, J.-F., Relative basicities toward metal triflates Lewis acids by electrospray mass spectrometry, Chem. Commun. 2010, 46, 8472-8474 link
  • Dia, R.-M. ; Belaqziz, R. ; Romane, A. ; Antoniotti, S. ; Dunach, E., Flavouring and odorant thiols from renewable natural resources by InIII-catalysed hydrothioacetylation and lipase-catalysed solvolysis, Tetrahedron Lett. 2010, 51, 2164-2167 link
  • Bouzroura, S. ; Bentarzi, Y. ; Kaoua, R. ; Nedjar-Kolli, B. ; Poulain-Martini, S. ; Dunach, E., A convenient one pot preparation of 4-thiazolidinones from enaminolactones, Org. Commun. 2010, 3, 8-14. link
  • Ben, O. R. ; Affani, R. ; Tranchant, M.-J. ; Antoniotti, S. ; Dalla, V. ; Dunach, N-Acyliminium ion chemistry : highly efficient and versatile carbon-carbon bond formation by nucleophilic substitution of hydroxy groups catalyzed by Sn(NTf(2))(4), E. Angew. Chem., Int. Ed. 2010, 49, 776-80 link
  • Antoniotti, S. ; Poulain-Martini, S. ; Dunach, E., Electrophilic functionalization of non-activated olefins catalyzed by Lewis superacids, Synlett 2010, 2973-2988 link
  • Antoniotti, S. ; Dalla, V. ; Dunach, E., Metal triflimidates. Better than metal triflates as catalysts in organic synthesis. The effect of a highly delocalized counteranion, Angew. Chem., Int. Ed. 2010, 49, 7860-7888 link
Brevets_______________________________________________

« Préparation de sels métalliques de l’acide triflique et de l’acide triflimidique sous ultrasons ». J. R. Desmurs, E. Dunach, S. Olivero, S. Antoniotti. CDP-Innovation, PCT/FB2009/052 106 ; PCT Int. Appl. (2010), WO 2010055245 A2 20100520.

« Preparation of metal salts of triflic acid and of triflimidic acid by ultrasonic treatment. » , J. R Desmurs, E. Dunach, S. Olivero, S. Antoniotti. PCT Int. Appl. (2012), WO 2012010752 A1 20120126.

« Alcool Polyvinylique Fonctionnalisé par un dérivé Aromatique et/ou un dérivé Aliphatique », E. Delattre, B. Bouley, J. R. Desmurs, E. Dunach, G. Lemière. FR 9.10.2013 n° 13 59771.

« Nouveaux polymères contenant des sels de lithium ou de sodium de bis(sulfonyl)imides greffes, leurs procedes de preparation et leurs utilisations comme electrolytes pour batteries .» V. Morizur, S. Olivero, P. Knauth, J. R. Desmurs, E. Dunach, CDP-Innovation ; PCT WO2016/012670 du 28/01/2016 ; US20170170516A1

« Nouveaux polymères contenant des sels de lithium ou de sodium de sulfonamides, leurs procedes de preparation et leurs utilisations comme electrolytes pour batteries. » « Polymers containing lithium or sodium sulfonamide salts, their methods of preparation and their uses as electrolytes for batteries ». V. Morizur, S. Olivero, J. R. Desmurs, E. Dunach, CDP-Innovation. EP15763958.4 ; PCT WO2016/012669 du 28/01/2016 ; US20170179526A1.

« Nouveaux polymères contenant des fonctions sulfonates d’ammonium, leur procédés de préparation et leurs utilisation comme catalyseurs, antibactériens, fongicides ». V. Morizur, S. Olivero, J.R. Desmurs, E. Duñach, FR 14/02989, 2014.

« Nouveaux polymères contenant des fonctions sulfonates métalliques, leur procédés de préparation et leurs utilisation comme antibactériens, fongicides et antimicrobiens ». V. Morizur, S. Olivero, A. Adao, J.R. Desmurs, E. Duñach. FR 3030534B1 du 12/05/2017 ; EP3237490.

« Nouveaux polymères contenant des fonctions sulfonates métalliques, leur procédés de préparation et leurs utilisation comme catalyseurs ». V. Morizur, S. Olivero, J.R. Desmurs, E. Duñach. PCT/FR15/000238 du 22/12/2015.

« Nouvaux matériaux à effets optiques et leurs applications ». V. Morizur, S. Olivero, J.R. Desmurs, E. Duñach, Fr Dépôt Fév. 2017.