Vile, G.; Perez-Ramirez, J.; Nanoscale, 2014, 6, 13476-13482
Synthesis of riboflavines, quinoxalinones and benzodiazepines through chemoselective flow based hydrogenations
Baumann, M.; Baxendale, I. R.; Hornung, C. H.; Ley, S. V.; Rojo, M. V; Roper, K. A.; Molecules, 2014, 19(7), 9736-9759
Towards the development of chromone-based MEK1/2 modulators
Redwan, I. N.; Dyrager, C.; Solano, C.; de Troconiz, G. F.; Voisin, L.; Bliman, D.; Meloche, S.; Grotli, M.; Eur. J. Med. Chem., 2014, 85, 127-138
Synthesis of the tetrasaccharide repeating unit of the O-glycan from the polar flagellum flagellin of Azospirillum brasilense Sp7
Pal, K. B.; Mukhopadhyay, B.; Carbohydrate Research, 2014, 400, 9-13
Microreactors for peptide synthesis: looking through the eyes of twenty first century !!!
Ramesh, S.; Cherkupally, P.; de la Torre, B. G.; Govender, T.; Kruger, H. G.; Albericio, F.; Amino Acids, 2014, 46, 2091-2104
Chemical synthesis of a tetrasaccharide related to the exocellular polysaccharide from Rhodococcus sp. RHA1
Budhadev, D.; Mukhopadhyay, B.; Carbohydrate Research, 2014, 394, 26-31
FeNi nanoparticles with carbon armor as sustainable hydrogenation catalysts: towards biorefineries
Chieffi, G.; Giordano, C.; Antonietti, M.; Esposito, D.; Journal of Materials Chemistry A, 2014, 2, 11591-11596
Easy access to Ni3N- and Ni-carbon nanocomposite catalysts
Clavel, G.; Molinari, V.; Kraupner, A.; Giordano, C.; Chem. Eur. J., 2014, 20(29), 9018-9023
Stereo‐ and chemoselective character of supported CeO2 catalysts for continuous‐flow three‐phase alkyne hydrogenation
Vile, G.; Wrabetz, S.; Floryan, L.; Schuster, M. E.; Girgsdies, F.; Teschner, D.; Perez-Ramirez, J.; ChemCatChem, 2014, 6(7), 1928-1934
Green chemistry articles of interest to the pharmaceutical industry
Andrews, I.; Dunn, P.; Hayler, J.; Himkley, B.; Hughes, D.; Kaptein, B.; Lorenz, K.; Methew, S.; Rammeloo, T.; Wang, L.; Wells, A.; White, T. D.; Org. Process Res. Dev., 2011, 15, 748-756