Cloutier, M.; Muru, K.; Ravicoularamin, G.; Gauthier, C.; Nat. Prod. Rep., 2018, 35, 1251-1293
Single-atom heterogeneous catalysts based on distinct carbon nitride scaffolds
Chen, Z.; Vorobyeva, E.; Mitchell, S.; Fako, E.; Lopez, N.; Collins, S. M.; Leary, R. K.; Midgley, P. A.; Hauert, R.; Perez-Ramirez, J.; National Science Review, 2018, 5(5), 642-652
Selective ensembles in supported palladium sulfide nanoparticles for alkyne semi-hydrogenation
Albani, D.; Shahrokhi, M.; Chen, Z.; Mitchell, S.; Hauert, R.; Lopez, N.; Perez-Ramirez, J.; Nature Communications, 2018, 9, article number: 2634
The dual reactivity of Weinreb amides applied to the late-stage divergent functionalisation of meso pyrrolidines
Boufroura, H.; Sevaille, L.; Gigant, N.; Drege, E.; Joseph, D.; New J. Chem., 2018, 42, 12403-12411
The renascence of continuous-flow peptide synthesis – an abridged account of solid and solution-based approaches
Gordon, P. C.; Org. Biomol. Chem., 2018, 16, 180-196
Discovery of a novel chemotype of histone lysine methyltransferase EHMT1/2 (GLP/G9a) inhibitors: rational design, synthesis, biological evaluation and cocrystal structure
Milite, C.; Feoli, A.; Horton, J. R.; Rescigno, D.; Cipriano, A.; Pisapia, V.; Viviano, M.; Pepe, G.; Amendola, G.; Novellino, E.; Cosconati, S.; Cheng, X.; Castellano, S.; Sbardella, G.; J. Med. Chem., 2019, 62(5), 2666-2689
Catalytic hydrogenolysis of substituted diaryl ethers by using ruthenium nanoparticles on an acidic supported ionic liquid phase (Ru@SILP-SO3H)
Rengshausen, S.; Etscheidt, F.; Großkurth, J.; Luska, K. L.; Bordet, A.; Leitner, W.; Synlett, 2019, 30(4), 405-412
Prodrugs for colon-restricted delivery: Design, synthesis, and in vivo evaluation of colony stimulating factor 1 receptor (CSF1R) inhibitors
George, D. M.; Huntley, R. J.; Cusack, K.; Duignan, D. B.; Hoemann, M.; Loud, J.; Mario, R.; Melim, T.; Mullen, K.; Somal, G.; Wang, L.; Edmunds, J. J.; PlosOne, 2018, online article
Catalytic oxidation of aqueous bioethanol: an efficient upgrade from batch to flow
Mostrou, S.; Sipocz, T.; Nagl, A.; Fodi, B.; Darvas, F.; Fottinger, K.; van Bokhoven, J. A.; React. Chem. Eng., 2018, 3, 781-789
Continuous-flow reductive alkylation: synthesis of bio-based symmetrical and disymmetrical ethers
Bruniaux, S.; Luart, D.; Len, C.; Synthesis, 2018, 50, 1849-1856