2020
· 102. “Preparation of Chiral Photosensitive Organocatalysts and Their Application for the Enantioselective Synthesis of 1,2-Diamines"
Lyu, J.; Claraz, A.; Vitale, M. R.; Allain, C.; Masson, G. J. Org. Chem., 2020, 85, 12843–12855. DOI 10.1021/acs.joc.0c01931
· 101. “La Chimie Organique en France: Une Longue Tradition qui Persiste!"
Masson, G. J. Org. Chem., 2020, 85, 11589–11591. DOI 10.1021/acs.joc.0c02019
· 100. “A straightforward synthesis of a new family of molecules: 2,5,8-trialkoxyheptazines. Application to photoredox catalyzed transformations"
Le, T.; Galmiche, L.; Masson, G.; Allain, C; Audebert, P. Chem. Commun., 2020, 56, 10742-10745. DOI 10.1039/D0CC05118G
· 99. “Tritylium assisted iodine catalysis for the synthesis of unsymmetrical triarylmethanes"
Courant, T.; Lombard, M.; Boyarskaya, D. V.; Neuville, L.; Masson, G. Org. Biomol. Chem., 2020, 18, 6502-6508. DOI 10.1039/D0OB01502D
· 98. “Selective Double C–H Functionalization: A 4-Component Catellani Reaction"
Varlet, T.; Neuville, L.; Masson, G. Chem, 2020, 6, 1855-1858. DOI 10.1016/j.chempr.2020.07.020
· 97. “Chemical Photocatalysis – Do It Right!"
Masson, G.; König, B. ChemPhotoChem, 2020, Special Issue: Photochemical Synthesis, 1191–1192. DOI 10.1002/ejoc.201901828
· 96. “Enantioselective Redox‐Divergent Chiral Phosphoric Acid Catalyzed Quinone Diels-Alder Reactions"
Varlet, T.; Gelis, C.; Retailleau, P.; Bernardat, G.; Neuville, L.; Masson, G. Angew. Chem. Int. Ed., 2020, 59, 8491-8496. DOI 10.1002/anie.202000838
· 95. “Electrochemical Intramolecular Oxytrifluoromethylation of N-Tethered Alkenyl Alcohols: Synthesis of Functionalized Morpholines"
Claraz, A.; Courant, T.; Masson, G. Org. Lett., 2020, 22, 1580–1584. DOI 10.1021/acs.orglett.0c00176
· 94. “Enantioselective synthesis of complex fused heterocycles via chiral phosphoric‐acid catalyzed intramolecular inverse‐electron demand aza‐Diels‐Alder reaction"
Jarrige, L.; Gandon, V.; Masson, G. Chem. Eur. J., 2020, 26, 1406-1413. DOI 10.1002/chem.201904902
2019
· 93. “s-Tetrazine Dyes: A Facile Generation of Photoredox Organocatalysts for Routine Oxidations"
Le, T.; Courant, T.; Merad, J.; Allain, C.; Audebert, P.; Masson, G. J. Org. Chem., 2019, 84, 16139–16146. DOI 10.1021/acs.joc.9b02454
· 92. “Aerobic Tetrazine‐Catalyzed Oxidative Nitroso‐Diels‐Alder Reaction of N‐Arylhydroxylamines with Dienecarbamates: Access to Functionalized 1,6‐Dihydro‐1,2‐oxazines"
Le, T.; Courant, T.; Merad, J.; Allain, C.; Audebert, P.; Masson, G. ChemCatChem, 2019, 7, 5282–5286. DOI 10.1021/acs.joc.9b02454
· 91. “Combining Organocatalysis and Photoredox Catalysis: An Asymmetric Synthesis of Chiral β-Amino α-Substituted Tryptamines"
Levitre, G.; Audubert, C.; Dumoulin, A.; Goual, N.; Retailleau, P.; Moreau, X.; Masson, G. ChemCatChem, 2019, 11, 5723-5727. DOI 10.1002/cctc.201901266
· 90. "Four-Component Photoredox-Mediated Azidoalkoxy-trifluoromethylation of Alkenes"
Levitre, G.; Dagousset, G.; Anselmi, E.; Tuccio, B.; Magnier, E.; Masson, G. Org. Lett., 2019, 21, 6005-6010. DOI 10.1021/acs.orglett.9b02152
· 89. "Tandem Chiral Cu(II) Phosphate-Catalyzed Deoxygenation of Nitrones/Enantioselective Povarov Reaction with Enecarbamates"
Gelis, C.; Levitre, G.; Guerineau, V.; Touboul, D.; Neuville, L.; Masson, G. Eur. J. Org. Chem., 2019, 31, 5151-5155. DOI 10.1002/ejoc.201900547
· 88. “Chiral Phosphoric Acid-Catalyzed Enantioselective Construction of Structurally Diverse Benzothiazolopyrimidines"
Jarrige, L.; Glavač, D.; Levitre, G.; Retailleau, P.; Bernadat, G.; Neuville, L.; Masson, G. Chem. Sci., 2019, 10, 3765-3769. DOI 10.1039/C8SC05581E
· 87. “Catalyst-free cycloaddition of 1,3-diene-1-carbamates with azodicarboxylates: A rapid click reaction"
Varlet, T.; Levitre, G.; Retailleau, P.; Masson, G. Bioorg. Med. Chem. 2019, 27, 2438-2443. DOI 10.1016/j.bmc.2019.02.008
· 86. "2nd PSL Chemical Biology Symposium (2019): At the Crossroads of Chemistry and Biology"
Lucchino, M.; Billet, A.; Versini, A.; Bavireddi, H.; Dasari, B.-D.; Debieu, S.; Colombeau, L.; Caneque, T.; Wagner, A.; Masson, G.; Taran, F.; Karoyan, P.; Delepierre, M.; Gaillet, C.; Houdusse, A.; Britton, S.; Schimdt, F.; Florent, J.-C.; Belmont, P.; Monchaud, D.; Cossy, J.; Thomas, C.; Gautier, A.; Johannes, L.; Rodiguez, R.; ChemBioChem, 2019, 20, 968
2018
· 85. “Ultrafast Maximum‐Quantum NMR Spectroscopy for the Analysis of Aromatic Mixtures"
Concilio, M. G.; Jacquemmoz, C.; Boyarskaya, D.; Masson, G.; Dumez, J. N. ChemPhysChem., 2018, 19, 3310-3317. DOI 10.1002/cphc.201800667
· 84. “Visible light-triggered C-C and C-N bonds formation by C-S bonds cleavage of benzylic thioethers"
Lanzi, M.; Merad, J.; Boyarskaya, D. V., Maestri, G.; Allain, C.; Masson, G. Org. Lett., 2018, 20, 5247-5250. DOI 10.1021/acs.orglett.8b02196
· 83. “Highly Diastereo‐ and Enantioselective Synthesis of Cyclo‐hepta[b]indoles via Chiral Phosphoric Acid‐Catalyzed (4 + 3)‐Cycloaddition"
Gelis, C.; Levitre, G.; Merad, J.; Retailleau, P.; Neuville, L.; Masson, G. Angew. Chem. Int. Ed., 2018, 57, 12121-12125. DOI 10.1002/anie.201807069
· 82. “Stereoselectivity Switch in the Trapping of Polar Organometallics with Andersen’s Reagent—Access to Highly Stereoenriched Transformable Biphenyls"
Levitre, G.; Fer, M. J.; Berreur, J.; Masson, G.; Panossian, A.; Leroux, F. R. J. Org. Chem., 2018, 83, 7751-7761. DOI 10.1021/acs.joc.8b00648
· 81. “Asymmetric iodine catalysis-mediated enantioselective oxidative transformations"
Claraz, A.; Masson, G. Org. Biomol. Chem., 2018, 16, 5386-5402. DOI 10.1039/C8OB01378K
· 80. “L’organocatalyse énantiosélective : moderne, efficace et propre"
Jarrige, L.; Masson, G. Actualité chimique, 2018, 426, 63-64.
· 79. “Brønsted Acid Catalysis as a Tool for the Synthesis of Natural Products and Pharmaceuticals"
Merad, J.; Lalli, C.; Bernadat, G.; Maury, J.; Masson, G. Chem. Eur. J., 2018, 24, 3925-3943. DOI 10.1002/chem.201703556
2017
· 78. “Asymmetric α-Sulfonyl- and α-Phosphoryl-Oxylation of Ketones by a Chiral Hypervalent Iodine(III)"
Levitre, G.; Dumoulin, A.; Retailleau, P.; Panossian, A.; Leroux, F. R.; Masson, G. J. Org. Chem., 2017, 82, 11877-11883. DOI 10.1021/acs.joc.7b01597
· 77. “Enantioselective Organocatalytic Intramolecular aza-Diels–Alder Reaction"
Jarrige, L.; Blanchard, F. ; Masson, G. Angew. Chem. Int. Ed. 2017, 56, 10573-10576. DOI 10.1002/anie.201705746
· 76. “Easy Access to Biologically Active Quinolin-2(1H)-ones via a One-Pot Tandem-oxa-Michael–Aldol Sequence"
Jarrige, L.; Merad, J.; Zaied, S.; Blanchard, F.; Masson, G. Synlett, 2017, 28, 1724-1728. DOI 10.1055/s-0036-1588470
· 75. “Fluorinated Sulfilimino Iminiums: Efficient and Versatile Sources of Perfluoroalkyl Radicals under Photoredox Catalysis"
Daniel, M.; Dagousset, G.; Diter, P.; Klein, P.-A.; Tuccio, B.; Goncalves, A.-M.; Masson, G.; Magnier, E. Angew. Chem. Int. Ed., 2017, 56, 3997-4001. DOI 10.1002/anie.201700290
· 74. “Enantioselective Three-Component Amination of Enecarbamates Enables the Synthesis of Structurally Complex Small Molecules" Dumoulin, A.; Bernadat, G.; Masson, G. J. Org. Chem., 2017, 82, 1775–1789. DOI 10.1021/acs.joc.6b03093
· 73. “Chiral Hypervalent Iodine(III) Catalyst Promotes Highly Enantioselec-tive Sulfonyloxy- and Phosphoryloxy-Lactonizations"
Gelis, C.; Dumoulin, A.; Bekkaye, M.; Neuville, L.; Masson, G. Org. Lett., 2017, 19, 278–281. DOI 10.1021/acs.orglett.6b03631
· 72. “Visible Light Photoredox-Mediated Oxidative Tandem Nitroso Diels-Alder Reaction of Arylhydroxylamines with Conjugated Dienes" Santacroce, V.; Duboc, R.; Malacria, M.; Maestri, G.; Masson, G. Eur. J. Org. Chem., 2017, 15, 2095–2098. DOI 10.1002/ejoc.201601492
2016
· 71. “Asymmetric Oxidative Nitroso-Diels–Alder Reaction of N-Arylhydroxylamines Catalyzed by a Chiral Phosphoric Acid"
Dumoulin, A.; Masson, G. J. Org. Chem., 2016, 21, 10154–10159. DOI 10.1021/acs.joc.6b01256
· 70. "Recent Progress in Visible-Light Photoredox-Catalyzed Intermolecular 1,2-Difunctionalization of Double Bonds via an ATRA-Type Mechanism"
Courant T.; Masson, G. J. Org. Chem., 2016, 81, 6945-6952. DOI 10.1021/acs.joc.6b01058
· 69. "Visible-Light Photoredox-Catalyzed Coupling Reaction of Azoles with α-Carbamoyl Sulfides"
Jarrige, L.; Levitre, G.; Masson, G. J. Org. Chem., 2016, 81, 7230-7236. DOI 10.1021/acs.joc.6b01108
· 68. "Chiral Phosphoric Acid Catalyzed [3 + 2] Cycloaddition and Tandem Oxidative [3 + 2] Cycloaddition: Asymmetric Synthesis of Substituted 3-Aminodihydrobenzofurans"
Gelis, C.; Bekkaye, M.; Lebée, C.; Blanchard, F.; Masson, G. Org. Lett., 2016, 18, 3422–3425. DOI 10.1021/acs.orglett.6b01593
· 67. "Photoredox-Catalyzed Three-Component Tandem Process: An Assembly of Complex Trifluoromethylated Phthalans and Isoindolines"
Jarrige, L.; Carboni, A.; Dagousset, G.; Levitre, G.; Magnier, E.; Masson, G. Org. Lett., 2016, 18, 2906–2909. DOI 10.1021/acs.orglett.6b01257
· 66. "α-Carbamoylsulfides as N-Carbamoylimine Precursors in the Visible Light Photoredox-Catalyzed Synthesis of α,α-Disubstituted Amines"
Lebée, C.; Languet, M.; Allain, C.; Masson, G. Org. Lett., 2016, 18, 1478–1481. DOI 10.1021/acs.orglett.6b00442
· 65. "Lewis acids turn unreactive substrates into pure enantiomers"
Dumoulin, A.; Masson, G. Science, 2016, 351, 918-919. DOI 10.1126/science.aaf2577
· 64. "Highly enantioselective intermolecular iodo- and chloroamination of enecarbamates catalyzed by chiral phosphoric acids or calcium phosphate salts"
Lebée, C.; Blanchard, F.; Masson, G. Synlett, 2016, 27, 559-563. DOI: 10.1055/s-0035-1650585
· 63. "Synthesis of new axially chiral iodoarenes"
Bekkaye, M.; Masson, G. Synthesis 2016, 48, 302-312. DOI 10.1055/s-0035-1560512