2020
“Endocyclic Enamides Derived from Aza-Diketopiperazines as Olefin Partners in Povarov Reaction: An Access to Tetracyclic N-Heterocycles ” ,
T. Maujean, I. Chataigner, N. Girard, M. Gulea, D. Bonnet
Eur. J. Org. Chem. 2020.
DOI:10.1002/ejoc.202001339
"Insights into the Ochratoxin A/Aptamer Interactions on a Functionalized Silicon Surface by Fourier Transform Infrared and UV–Vis Studies",
T. Aschl, G. Frison, A. Moraillon, F. Ozanam, P. Allongue, A.-C. Gouget-Laemmel
Langmuir, 2020.
DOI:10.1021/acs.langmuir.0c02358
“Selective Formation of Epoxylimonene catalyzed by Phosphonyle/Arsonyle Derivatives of trivacant polyoxotungstates at low temperature ” ,
O. Makrygenni, L. Vanmairis, S. Taourit, F. Launay, A. Shum Cheong Sing, A. Proust, H. Gérard, R. Villanneau
Eur. J. Inorg. Chem., 2020, 605-612.
DOI: 10.1002/ejic.201901152
“Ligand effects on coordination properties of organolithium compounds: insights from computational experiments on a “weakened” Li+ ” ,
H. Gérard, P. Chaquin, J. Maddaluno
J. Mol. Model. 2020, 26, 59.
DOI: 10.1007/s00894-020-4302-2
“Bromine-lithium exchange on gem-dibromoalkenes. Part 1: batch vs microflow conditions” ,
B. Picard, K. Perez, T. Lebleu, D. Vuluga, F. Burel, D.C. Harrowven, I. Chataigner, J. Maddaluno, J. Legros
J. Flow. Chem. 2020, 10, 139-143.
DOI:10.1007/s41981-019-00057-6
“Dearomatization of 3-Cyanoindoles by (3+2) Cycloaddition: From Batch to Flow Chemistry” ,
M. Mannveau, S. Tanii, F. Gens, J. Legros, I. Chataigner
Org. Biomol. Chem. 2020, 18, 3481-3486.
DOI:10.1039/D0OB00582G
“Bromine-lithium exchange on a gem-dibromoalkene - Part 2: comparative performance of flow micromixers” ,
K. Pérez, B. Picard, D. Vuluga, F. Burel, R. Hreiz, L.Falk, J.-M..Commenge, A. Nagaki, J. Yoshida, I. Chataigner, J. Maddaluno, J. Legros
J. Org. Process. Res. Dev. 2020,24, 787-791.
DOI:10.1021/acs.oprd.0c00203
“Solvation Effects Drive the Selectivity in Diels-Alder Reaction Under Hyperbaric Conditions ” ,
D. Loco, R. Spezia, F. Cartier, I. Chataigner, J.-P. Piquemal
Chem. Commun. 2020, 56, 6632-6635.
DOI: 10.1039/D0CC01938K
2019
“Direct Synthesis of Nitriles from Carboxylic Acids Using Indium Catalyzed Transnitrilation: Mechanistic and Kinetic Study” ,
L. Vanoye, A. Hammoud, H. Gérard, A. Barnes, R. Philippe, P. Fongarland, C. de Bellefon, A. Favre-Réguillon,
ACS Catal., 2019, 9, 9705-9714.
DOI:10.1021/acscatal.9b02779
“Role of Oleylamine Revisited: An Original Disproportionation Route to Monodispersed Cobalt and Nickel Nanocrystals” ,
A. Vivien, M. Guillaumont, L. Meziane, C. Salzemann, C. Aubert, S. Halbert, H. Gérard, M. Petit, C. Petit,
Chem. Mater., 2019,31, 960-968.
DOI: 10.1021/acs.chemmater.8b04435
“Dearomatization of 3-Nitroindoles with Highly γ-Functionalized Allenoates in Formal (3+2) Cycloadditions” ,
L. Birbaum, L. Gillard, H. Gérard, H. Oulyadi, G. Vincent, X. Moreau, M. De Paolis, I. Chataigner,
Chem. Eur. J., 2019,25, 13688-13693.
DOI:10.1002/chem.201903455
“Catalytically active species in Copper/DiPPAM‐Catalyzed 1,6‐Asymmetric Conjugate Addition of Dialkylzinc to Dienones: a computational overview” ,
S. Halbert, J. Lauberteaux, C. Blons, R. Marcia de Figueiredo, C. Crévisy, O. Baslé, J.-M. Campagne, M. Mauduit, H. Gérard,
ChemCatChem, 2019, 11, 4108-4115.
DOI:10.1002/cctc.201900233
“Confronting the Re-emergence of Chemical Weapons New Instruments in the Chemist’s Toolbox” ,
B. Picard, I. Chataigner, J. Maddaluno, J. Legros,
Org. Biomol. Chem., 2019, 17, 6528-6537.
DOI:10.1039/C9OB00802K
“Facile dearomatization of nitroaromatic compounds using lithium enolates of unsaturated ketones in conjugate additions and (4+2) formal cycloadditions ” ,
K. Pasturaud, B. Rkein, M. Sanselme, M. Sebban, S. Lakhdar, M. Durandetti, J. Legros, I. Chataigner,
Chem. Commun., 2019, 55, 6528-6537.
DOI:10.1039/C9CC02924A
“Fused Hexacyclic Ring System Through Interrupted iso-Nazarov Initiated Diastereoselective Domino Polycyclization of 2,4-Dienals ” ,
A.-S. Marques, T. Duhail, J. Marrot, I. Chataigner, V. Coeffard, G. Vincent, X. Moreau,
Angew. Chem. Int. Ed., 2019, 58, 9969-9973.
DOI:10.1002/anie.201903860