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Stereoselective total synthesis of the marine macrolide sanctolide A
Yadav, J. S.; Suresh, B.; Srihari, P.; Eur. J. Org. Chem., 2015, 2015(26), 5856-5863
Selective liquid‐phase hydrogenation of a nitro group in substituted nitrobenzenes over Au/Al2O3 catalyst in a packed‐bed flow reactor
Nuzhdin, A. L.; Moroz, B. L.; Bukhtiyarova, G. A.; Reshetnikov, S. I.; Pyrjaev, P. A.; Aleksandrov P. V.; Bukhtiyarov, V. I.; ChemPlusChem, 2015, 80(12), 1741-1749
Flow chemistry vs. flow analysis
Trojanowicz, M.; Talanta, 2016, 146, 621-640
Structural identification of petroleum acids by conversion to hydrocarbons and multidimensional gas chromatography-mass spectrometry
Wilde, M. J.; Rowland S. J.; Analytical Chemistry, 2015, 87(16), 8457-8465
Monitoring glycan-protein interactions by NMR spectroscopic analysis: A simple chemical tag that mimics natural CH–π interactions
Calle, L. P.; Echeverria, B.; Franconetti, A.; Serna, S.; Fernandez-Alonso, M. C.; Diercks, T.; Canada, F. J.; Arda, A.; Reichardt, N. C.; Jimenez-Barbero, J.; Chem. Eur. J., 2015, 21(32), 11408-11416
An efficient and more sustainable one-step continuous-flow multicomponent synthesis approach to chromene derivatives
Vaddula, B. R.; Yalla, S.; Gonzalez, M. A.; J. Flow Chem., 2015, 5(3), 172-177
The expanding utility of continuous flow hydrogenation
Cossar, P. J.; Hizartzidis, L.; Simone, M. I.; McCluskey A.; Gordon, C. P.; Org. Biomol. Chem., 2015, 13, 7119-7130
Structure-based optimization of naphthyridones into potent ATAD2 bromodomain inhibitors
Bamborough, P.; Chung, C.; Furze, R. C.; Grandi, P.; Michon, A.; Sheppard, R. J.; Barnett, H.; Diallo, H.; Dixon, D. P.; Douault, C.; Jones, E. J.; Karamshi, B.; Mitchell, D. J.; Prinjha, R. K.; Rau, C.; Watson, R. J.; Werner, T.; Demont, E. H.; J. Med. Chem., 2015, 58(15), 6151-6178
Enantiodivergent synthesis of bis-spiropyrrolidines via sequential interrupted and completed (3+2) cycloadditions
Conde, E.; Rivilla, I.; Larumbe, A.; Cossio F. P.; J. Org. Chem., 2015, 80(23), 11755-11767