A prototype device for evaporation in batch and flow chemical processes
暂无分享,去创建一个
Claudio Battilocchio | Steven V. Ley | S. Ley | C. Battilocchio | Benjamin J. Deadman | Eric Sliwinski | É. Sliwiński | Claudio Battilocchio
[1] Claudio Battilocchio,et al. A Flow-Based Synthesis of 2-Aminoadamantane-2-carboxylic Acid , 2012 .
[2] Steven V. Ley,et al. Hydrogenation in flow: Homogeneous and heterogeneous catalysis using Teflon AF-2400 to effect gas-liquid contact at elevated pressure†‡ , 2011 .
[3] S. Arseniyadis,et al. Modern tools for the synthesis of complex bioactive molecules , 2012 .
[4] Marielle M. E. Delville,et al. Continuous flow production of thermally unstable intermediates in a microreactor with inline ir-analysis: Controlled vilsmeier-haack formylation of electron-rich arenes , 2012 .
[5] Steven V. Ley,et al. A breakthrough method for the accurate addition of reagents in multi-step segmented flow processing† , 2011 .
[6] R. C. Weast. CRC Handbook of Chemistry and Physics , 1973 .
[7] J. Edel,et al. Microfluidic evaporator for on-chip sample concentration. , 2012, Lab on a chip.
[8] M. Lakshmi Kantam,et al. One-pot synthesis of conjugated nitroalkenes by diamino-functionalised mesoporous material , 1999 .
[9] F. Bigi,et al. Supported organic catalysts: synthesis of (E)-nitrostyrenes from nitroalkanes and aromatic aldehydes over propylamine supported on MCM-41 silica as a reusable catalyst , 2001 .
[10] S. Kato,et al. Vacuum membrane distillation on a microfluidic chip. , 2009, Chemical communications.
[11] Chunhua Wang,et al. Synthesis, characterization and catalytic application of bifunctional catalyst: Al-MCM-41-NH2 , 2011 .
[12] Steven V. Ley,et al. ReactIR Flow Cell: A New Analytical Tool for Continuous Flow Chemical Processing , 2010 .
[13] P. Tabeling,et al. Microevaporators for kinetic exploration of phase diagrams. , 2006, Physical review letters.
[14] Steven V Ley,et al. On being green: can flow chemistry help? , 2012, Chemical record.
[15] Y. Iwasawa,et al. Heterogeneous organic base-catalyzed reactions enhanced by acid supports. , 2007, Journal of the American Chemical Society.
[16] Claudio Battilocchio,et al. A machine-assisted flow synthesis of SR48692: a probe for the investigation of neurotensin receptor-1. , 2013, Chemistry.
[17] D. T. McQuade,et al. Mechanism and application of a microcapsule enabled multicatalyst reaction. , 2007, Journal of the American Chemical Society.
[18] E. Hilmen,et al. Separation of azeotropic mixtures : tools for analysis and studies on batch distillation operation , 2000 .
[19] Steven V Ley,et al. An expeditious synthesis of imatinib and analogues utilising flow chemistry methods. , 2013, Organic & biomolecular chemistry.
[20] Peter J. Dunn,et al. Green chemistry tools to influence a medicinal chemistry and research chemistry based organisation , 2008 .
[21] Ryan L Hartman,et al. Multistep microchemical synthesis enabled by microfluidic distillation. , 2010, Angewandte Chemie.
[22] Y. Hashimoto,et al. Guanidine‐Thiourea Bifunctional Organocatalyst for the Asymmetric Henry (Nitroaldol) Reaction , 2005 .
[23] K. Jensen,et al. Heterogeneous catalysis with continuous flow microreactors , 2012 .
[24] N. R. Shiju,et al. Mesoporous Silica with Site-Isolated Amine and Phosphotungstic Acid Groups: A Solid Catalyst with Tunable Antagonistic Functions for One-Pot Tandem Reactions** , 2011, Angewandte Chemie.
[25] S. Loebbecke,et al. Use of immobilized organic base catalysts for continuous-flow fine chemical synthesis , 2008 .
[26] James G. Stevens,et al. The continuous self aldol condensation of propionaldehyde in supercritical carbon dioxide: a highly selective catalytic route to 2-methylpentenal , 2009 .
[27] Patrick S Doyle,et al. Permeation-driven flow in poly(dimethylsiloxane) microfluidic devices. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[28] Steven V Ley,et al. Continuous multiple liquid-liquid separation: diazotization of amino acids in flow. , 2012, Organic letters.
[29] Y. Iwasawa,et al. Cooperative catalysis of primary and tertiary amines immobilized on oxide surfaces for one-pot C-C bond forming reactions. , 2008, Angewandte Chemie.
[30] Ryan L Hartman,et al. Distillation in microchemical systems using capillary forces and segmented flow. , 2009, Lab on a chip.
[31] Andreas Kirschning,et al. Continuous flow techniques in organic synthesis. , 2003, Chemistry.
[32] Claudio Battilocchio,et al. A mild and efficient flow procedure for the transfer hydrogenation of ketones and aldehydes using hydrous zirconia. , 2013, Organic letters.
[33] S. Ley,et al. Teflon AF-2400 mediated gas-liquid contact in continuous flow methoxycarbonylations and in-line FTIR measurement of CO concentration. , 2011, Organic & biomolecular chemistry.
[34] T. Wirth,et al. Intelligent microflow: development of self-optimizing reaction systems. , 2011, Angewandte Chemie.
[35] D. Macquarrie,et al. Understanding the influence of the immobilization procedure on the catalytic activity of aminopropylsilicas in C_C forming reactions , 2003 .
[36] Carl J. Schaschke,et al. A Dictionary of Chemical Engineering , 2014 .
[37] Steven V Ley,et al. A flow-based synthesis of imatinib: the API of Gleevec. , 2010, Chemical communications.
[38] Steven V Ley,et al. Continuous flow reaction monitoring using an on-line miniature mass spectrometer. , 2012, Rapid communications in mass spectrometry : RCM.
[39] Steven V Ley,et al. The oxygen-mediated synthesis of 1,3-butadiynes in continuous flow: using Teflon AF-2400 to effect gas/liquid contact. , 2012, ChemSusChem.
[40] Takehiko Kitamori,et al. Microfluidic Distillation Utilizing Micro-Nano Combined Structure , 2008 .
[41] Steven V Ley,et al. A prototype continuous-flow liquid-liquid extraction system using open-source technology. , 2012, Organic & biomolecular chemistry.
[42] Victor Sans,et al. Base supported ionic liquid-like phases as catalysts for the batch and continuous-flow Henry reaction , 2008 .
[43] Kevin I Booker-Milburn,et al. Flow photochemistry: Old light through new windows , 2012, Beilstein journal of organic chemistry.
[44] Y. Gupta,et al. Mechanism of Amine Sensitization in Shocked Nitromethane , 1998 .
[45] A. Palmieri,et al. Use of heterogeneous catalyst KG-60-NEt2 in Michael and Henry reactions involving nitroalkanes , 2003 .
[46] Oliver Lade,et al. Nitrogen supported solvent evaporation using continuous-flow microfluidics , 2012 .
[47] Alessandro Palmieri,et al. Continuous flow based catch and release protocol for the synthesis of α-ketoesters , 2009, Beilstein journal of organic chemistry.
[48] Y. Iwasawa,et al. Organofunctionalized catalyst surfaces highly active and selective for carbon–carbon bond-forming reactions , 2009 .