Julie Oble
Affiliations: | 2008-2010 | chemistry | Sorbonne Université, Paris, France |
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Curpanen S, Reichert P, Lupidi G, et al. (2022) Modular synthesis of 2-furyl carbinols from 3-benzyldimethylsilylfurfural platforms relying on oxygen-assisted C-Si bond functionalization. Beilstein Journal of Organic Chemistry. 18: 1256-1263 |
Sala R, Kiala G, Veiros LF, et al. (2022) Redox-Neutral Ru(0)-Catalyzed Alkenylation of 2-Carboxaldimine-heterocyclopentadienes. The Journal of Organic Chemistry. 87: 4640-4648 |
Foschi F, Loro C, Sala R, et al. (2020) Intramolecular Aminoazidation of Unactivated Terminal Alkenes by Palladium-Catalyzed Reactions with Hydrogen Peroxide as the Oxidant. Organic Letters. 22: 1402-1406 |
Ravasco JMJM, Monteiro CM, Siopa F, et al. (2019) Creating Diversity from Biomass: A Tandem Bio/Metal-Catalysis towards Chemoselective Synthesis of Densely Substituted Furans. Chemsuschem |
Roudesly F, Veiros LF, Oble J, et al. (2018) Pd-Catalyzed Direct C-H Alkenylation and Allylation of Azine N-Oxides. Organic Letters. 20: 2346-2350 |
Lorion MM, Duarte FJ, Calhorda MJ, et al. (2016) Opening the Way to Catalytic Aminopalladation/Proxicyclic Dehydropalladation: Access to Methylidene γ-Lactams. Organic Letters. 18: 1020-3 |
Riflade B, Lachkar D, Oble J, et al. (2014) Pd-containing organopolyoxometalates derived from Dawson polyoxometalate [P₂W₁₅V₃O₆₂]⁹⁻: Lewis acidity and dual site catalysis. Organic Letters. 16: 3860-3 |
Rajabi J, Lorion MM, Ly VL, et al. (2014) Dormant versus evolving aminopalladated intermediates: toward a unified mechanistic scenario in Pd(II)-catalyzed aminations. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 1539-46 |
Lorion MM, Gasperini D, Oble J, et al. (2013) Palladium-catalyzed arylic/allylic aminations: permutable domino sequences for the synthesis of dihydroquinolines from Morita-Baylis-Hillman adducts. Organic Letters. 15: 3050-3 |
Oble J, Riflade B, Noël A, et al. (2011) Carbonyl-inserted organo-hybrids of a Dawson-type phosphovanadotungstate: scope and chemoselective oxidation catalysis. Organic Letters. 13: 5990-3 |