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Photooxygenation of an amino-thienopyridone yields a more potent PTP4A3 inhibitor
Salamoun, J. M.; McQueeney, K. E.; Patil, K.; Geib, S. J.; Sharlow, E. R.; Lazo, J. S.; Wipf, P.; Org. Biomol. Chem., 2016, 14(27), 6398-6402
New potent αvβ3 integrin ligands based on azabicycloalkane (γ,α)-dipeptide mimics
Pilkington-Miksa, M.; Araldi, E. M.; Arosio, D.; Belvisi, L.; Civera, M.; Manzoni, L.; Org. Biomol. Chem., 2016, 14(12), 3221-3233.
Library synthesis of cardiomyogenesis inducing compounds using an efficient two-step-one-flow process
Schon, M.; Dreier, D.; Schnurch, M.; Mihovilovic, M. D.; Monatsh. Chem., 2016, 147(3), 523-532
Contiuous-flow synthesis of deuterium-labeled antidiabetic chalcones: studies towards the selective deuteration of the alkynone core
Otvos, S. B.; Hsieh, C. T.; Wu, Y. C.; Li, J. H.; Chang, F. R.; Fulop, F.; Molecules, 2016, 21(3), 318-329
Synthesis of novel Iron(III) chelators based on triaza macrocycle backbone and 1-hydroxy-2(H)-pyridin-2-one coordinating groups and their evaluation as antimicrobial agents
Workman, D. G.; Hunter, M.; Dover, L. G.; Tetard, D.; Journal of Inorganic Biochemistry, 2016, 160, 49-58
Development of biolubricants from vegetable oils via chemical modification
McNutt, J.; He, Q.; J. Ind. Eng. Chem., 2016, 36, 1-12
Insights into the selective hydrogenation of levulinic acid to γ-valerolactone using supported mono- and bimetallic catalysts
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Total synthesis and biological evaluation of tubulysin analogues
Colombo, R.; Wang, Z.; Han, J.; Balachandran, R.; Daghestani, H. N.; Camarco, D. P.; Vogt, A.; Day, B. W.; Mendel, D.; Wipf, P.; J. Org. Chem., 2016, 81(21), 10302-10320
Optically pure, structural, and fluorescent analogues of a dimeric Y4 receptor agonist derived by an olefin metathesis approach
Liu, M.; Mountford, S. J.; Richardson, R. R.; Groenen, M.; Holliday, N. D.; Thompson, P. E.; J. Med. Chem., 2016, 59(13), 6059-6069