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Beilstein J. Org. Chem. 2017, 13, 1702–1709, doi:10.3762/bjoc.13.164
Graphical Abstract
Figure 1: Evolution of life from non-living, complex chemistry via chemical evolution of complex chemical com...
Figure 2: Schematic describing the evolutionary process. The inner circle represents the robotic process and ...
Figure 3: Recursive size-based selection and recirculation of droplets. Monodisperse droplets loaded with com...
Figure 4: Osmotic exchange and coarsening of co-incubating aqueous microdroplets. 50 mM glycylglycine and pur...
Figure 5: Real-time, LabVIEWTM tracking of osmosis-driven coarsening of 50 mM glycylglycine and pure water dr...
Figure 6: Process of the automated microfluidic platform, in which recursive evolution is applied at both ind...
Figure 7: The proposed device for droplet selection and evolution. The device is comprised of the following m...
Figure 8: Photographic images of individual microfluidic modules, fabricated our laboratory in PDMS from stan...
Beilstein J. Org. Chem. 2016, 12, 2776–2783, doi:10.3762/bjoc.12.276
Figure 1: Prusa i3 RepRap printer modified for the automated synthesis of ibuprofen. Left: Full view of robot...
Scheme 1: Synthetic route chosen for automated synthesis robot.
Figure 2: Top: The three reaction vessels printed for ibuprofen synthesis on different scales; bottom left: i...
Scheme 2: The digitisation of the synthesis of ibuprofen. This flow diagram shows the individual steps of the...
Beilstein J. Org. Chem. 2013, 9, 951–959, doi:10.3762/bjoc.9.109
Figure 1: Schematic representation of the 3D-printed reactionware devices employed in this work showing the i...
Figure 2: Flow system setup, where a R1 is connected to the syringe pumps and the ATR-IR flow cell with stand...
Figure 3: Carbonyl compounds and primary amines used in the syntheses reported in this work. Carbonyl compoun...
Figure 4: ATR-IR spectra of the synthesis of compounds 3b (on the left) and 3d (on the right). The spectrum o...
Figure 5: (a) IR spectra of benzaldehyde at different concentrations. The solvent peak at 1022 cm−1 remains c...
Figure 6: Comparison of the IR spectra of imine 3a, derived from benzaldehyde (1a) and aniline (2a), synthesi...
Figure 7: Representation of the setup for the two-step flow reaction employed in this work. The first reactor...
Figure 8: Example of an ATR-IR graph in which an imine spectrum is compared with the reduced imine spectrum.