The Use of Copper Flow Reactor Technology for the Continuous Synthesis of 1,4‐Disubstituted 1,2,3‐Triazoles
暂无分享,去创建一个
[1] J. Yoshida,et al. Aryllithium compounds bearing alkoxycarbonyl groups: generation and reactions using a microflow system. , 2008, Angewandte Chemie.
[2] Russell Dahl,et al. Rapid multistep synthesis of 1,2,4-oxadiazoles in a single continuous microreactor sequence. , 2008, The Journal of organic chemistry.
[3] Jun-ichi Yoshida,et al. Flash chemistry: fast chemical synthesis by using microreactors. , 2008, Chemistry.
[4] J. Yoshida,et al. Selective monolithiation of dibromobiaryls using microflow systems. , 2008, Organic letters.
[5] Rob C. Wheeler,et al. Continuous Flow Microwave-Assisted Reaction Optimization and Scale-Up Using Fluorous Spacer Technology , 2008 .
[6] Jacobus Johannes Maria Van Der Linden,et al. Investigation of the Moffatt−Swern Oxidation in a Continuous Flow Microreactor System , 2008 .
[7] B. Hamper,et al. Direct uncatalyzed amination of 2-chloropyridine using a flow reactor , 2007 .
[8] Simon J. F. Macdonald,et al. Mesoscale Flow Chemistry: A Plug-Flow Approach to Reaction Optimisation , 2007 .
[9] Christian H. Hornung,et al. A Microcapillary Flow Disc Reactor for Organic Synthesis , 2007 .
[10] Peng Wu,et al. Catalytic Azide—Alkyne Cycloaddition: Reactivity and Applications , 2007 .
[11] Jeremy L. Steinbacher,et al. Greener approaches to organic synthesis using microreactor technology. , 2007, Chemical reviews.
[12] A. Bogdan,et al. Improving solid-supported catalyst productivity by using simplified packed-bed microreactors. , 2007, Angewandte Chemie.
[13] Andreas Kirschning,et al. Combining enabling techniques in organic synthesis: continuous flow processes with heterogenized catalysts. , 2006, Chemistry.
[14] Masaaki Sato,et al. Low pressure Pd-catalyzed carbonylation in an ionic liquid using a multiphase microflow system. , 2006, Chemical communications.
[15] C. Stevens,et al. Study of the Baylis-Hillman reaction in a microreactor environment : first continuous production of Baylis-Hillman adducts , 2006 .
[16] J. Kobayashi,et al. Triphase Hydrogenation Reactions Utilizing Palladium‐Immobilized Capillary Column Reactors and a Demonstration of Suitability for Large Scale Synthesis , 2005 .
[17] Stefan Bräse,et al. Organic azides: an exploding diversity of a unique class of compounds. , 2005, Angewandte Chemie.
[18] S. Bräse,et al. Organische Azide – explodierende Vielfalt bei einer einzigartigen Substanzklasse , 2005 .
[19] Steven V Ley,et al. The use of a continuous flow-reactor employing a mixed hydrogen-liquid flow stream for the efficient reduction of imines to amines. , 2005, Chemical communications.
[20] J. Kobayashi,et al. Hydrogenation reactions using scCO2 as a solvent in microchannel reactors. , 2005, Chemical communications.
[21] Holger Löwe,et al. Development of Microstructured Reactors to Enable Organic Synthesis Rather than Subduing Chemistry , 2005 .
[22] Zoran Radić,et al. In situ selection of lead compounds by click chemistry: target-guided optimization of acetylcholinesterase inhibitors. , 2005, Journal of the American Chemical Society.
[23] M. Finn,et al. Mechanism of the ligand-free CuI-catalyzed azide-alkyne cycloaddition reaction. , 2005, Angewandte Chemie.
[24] M. Finn,et al. Head-to-tail peptide cyclodimerization by copper-catalyzed azide-alkyne cycloaddition. , 2005, Angewandte Chemie.
[25] S. Chittaboina,et al. One-pot synthesis of triazole-linked glycoconjugates , 2005 .
[26] K. Kacprzak. Efficient one-pot synthesis of 1,2,3-triazoles from benzyl and alkyl halides , 2005 .
[27] Volker Hessel,et al. Organic Synthesis with Microstructured Reactors , 2005 .
[28] F. Himo,et al. Copper(I)-catalyzed synthesis of azoles. DFT study predicts unprecedented reactivity and intermediates. , 2004, Journal of the American Chemical Society.
[29] W. Dehaen,et al. A microwave-assisted click chemistry synthesis of 1,4-disubstituted 1,2,3-triazoles via a copper(I)-catalyzed three-component reaction. , 2004, Organic letters.
[30] V. Fokin,et al. One-pot synthesis of 1,4-disubstituted 1,2,3-triazoles from in situ generated azides. , 2004, Organic letters.
[31] Craig J Hawker,et al. Efficiency and fidelity in a click-chemistry route to triazole dendrimers by the copper(i)-catalyzed ligation of azides and alkynes. , 2004, Angewandte Chemie.
[32] Rustem F Ismagilov,et al. Multi-step synthesis of nanoparticles performed on millisecond time scale in a microfluidic droplet-based system. , 2004, Lab on a chip.
[33] Takehiko Kitamori,et al. A Microfluidic Device for Conducting Gas-Liquid-Solid Hydrogenation Reactions , 2004, Science.
[34] Paul Watts,et al. Benchmarking of Microreactor Applications , 2004 .
[35] H. Kolb,et al. The growing impact of click chemistry on drug discovery. , 2003, Drug discovery today.
[36] Andreas Kirschning,et al. Continuous flow techniques in organic synthesis. , 2003, Chemistry.
[37] Helen Song,et al. Millisecond kinetics on a microfluidic chip using nanoliters of reagents. , 2003, Journal of the American Chemical Society.
[38] R. Ismagilov,et al. Screening of protein crystallization conditions on a microfluidic chip using nanoliter-size droplets. , 2003, Journal of the American Chemical Society.
[39] Philip Hodge,et al. Organic synthesis using polymer-supported reagents, catalysts and scavengers in simple laboratory flow systems. , 2003, Current opinion in chemical biology.
[40] Paul Watts,et al. Green chemistry: synthesis in micro reactors , 2003 .
[41] Helen Song,et al. A microfluidic system for controlling reaction networks in time. , 2003, Angewandte Chemie.
[42] Luke G Green,et al. A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. , 2002, Angewandte Chemie.
[43] M. Finn,et al. Click Chemistry: Diverse Chemical Function from a Few Good Reactions , 2001 .
[44] K. Sharpless,et al. Click-Chemie: diverse chemische Funktionalität mit einer Handvoll guter Reaktionen , 2001 .
[45] Joel Morris,et al. Substituent effects on the antibacterial activity of nitrogen-carbon-linked (azolylphenyl)oxazolidinones with expanded activity against the fastidious gram-negative organisms Haemophilus influenzae and Moraxella catarrhalis. , 2000, Journal of medicinal chemistry.
[46] E. De Clercq,et al. 1,2,3-Triazole-[2',5'-bis-O-(tert-butyldimethylsilyl)-beta-D- ribofuranosyl]-3'-spiro-5"-(4"-amino-1",2"-oxathiole 2",2"-dioxide) (TSAO) analogues: synthesis and anti-HIV-1 activity. , 1994, Journal of medicinal chemistry.
[47] D. Buckle,et al. Studies on 1,2,3-triazoles. 13. (Piperazinylalkoxy) [1]benzopyrano[2,3-d]-1,2,3-triazol-9(1H)-ones with combined H1-antihistamine and mast cell stabilizing properties. , 1986, Journal of medicinal chemistry.
[48] D. Buckle,et al. Studies on v-triazoles. 7. Antiallergic 9-oxo-1H,9H-benzopyrano[2,3-d]-v-triazoles. , 1983, Journal of medicinal chemistry.
[49] H. Hiemstra,et al. CuI‐Catalyzed Alkyne–Azide “Click” Cycloadditions from a Mechanistic and Synthetic Perspective , 2005 .
[50] H. Wamhoff. 4.11 – 1,2,3-Triazoles and their Benzo Derivatives , 1984 .