C-O bond Formation in a Microfluidic Reactor: High Yield SNAr Substitution of Heteroaryl Chlorides.
暂无分享,去创建一个
[1] A. Bogdan,et al. Nucleophilic aromatic substitution of heterocycles using a high-temperature and high-pressure flow reactor , 2016 .
[2] John Buckingham,et al. Dictionary of natural products , 2014 .
[3] S. Buchwald,et al. Highlights from the Flow Chemistry Literature 2013 (Part 1) , 2013, Journal of Flow Chemistry.
[4] A. Ritzén,et al. Continuous flow nucleophilic aromatic substitution with dimethylamine generated in situ by decomposition of DMF. , 2013, The Journal of organic chemistry.
[5] Klavs F. Jensen,et al. The role of flow in green chemistry and engineering , 2013 .
[6] Ruiwen Zhang,et al. Small-Molecule Inhibitor BMS-777607 Induces Breast Cancer Cell Polyploidy with Increased Resistance to Cytotoxic Chemotherapy Agents , 2013, Molecular Cancer Therapeutics.
[7] K. Jabran,et al. Application of bispyribac-sodium provides effective weed control in direct-planted rice on a sandy loam soil , 2012 .
[8] Steven V Ley,et al. On being green: can flow chemistry help? , 2012, Chemical record.
[9] Paul Watts,et al. Continuous flow reactors: a perspective , 2012 .
[10] C. Wiles,et al. Translation of microwave methodology to continuous flow for the efficient synthesis of diaryl ethers via a base-mediated SNAr reaction , 2011, Beilstein journal of organic chemistry.
[11] F. Darvas,et al. Stepwise aromatic nucleophilic substitution in continuous flow. Synthesis of an unsymmetrically substituted 3,5-diamino-benzonitrile library , 2011, Molecular Diversity.
[12] Steven V. Ley,et al. The flow synthesis of heterocycles for natural product and medicinal chemistry applications , 2011, Molecular Diversity.
[13] Timothy F. Jamison,et al. Continuous flow multi-step organic synthesis , 2010 .
[14] H. Neumann,et al. A general and efficient catalyst for palladium-catalyzed C-O coupling reactions of aryl halides with primary alcohols. , 2010, Journal of the American Chemical Society.
[15] J. Xu,et al. Copper(I)-catalyzed aryl bromides to form intermolecular and intramolecular carbon-oxygen bonds. , 2009, The Journal of organic chemistry.
[16] G. Sekar,et al. General, mild, and intermolecular Ullmann-type synthesis of diaryl and alkyl aryl ethers catalyzed by diol-copper(I) complex. , 2009, The Journal of organic chemistry.
[17] R. Mitra,et al. CuO nanoparticles catalyzed C-N, C-O, and C-S cross-coupling reactions: scope and mechanism. , 2009, The Journal of organic chemistry.
[18] J. Hartwig. Carbon–heteroatom bond formation catalysed by organometallic complexes , 2008, Nature.
[19] C. Wiles,et al. Continuous Flow Reactors, a Tool for the Modern Synthetic Chemist , 2008 .
[20] Phillip A Lichtor,et al. An improved Cu-based catalyst system for the reactions of alcohols with aryl halides. , 2008, The Journal of organic chemistry.
[21] Xin Lv,et al. A beta-keto ester as a novel, efficient, and versatile ligand for copper(I)-catalyzed C-N, C-O, and C-S coupling reactions. , 2007, The Journal of organic chemistry.
[22] Jeremy L. Steinbacher,et al. Greener approaches to organic synthesis using microreactor technology. , 2007, Chemical reviews.
[23] C. Dominguez,et al. Effect of microwave heating on Ullmann-type heterocycle-aryl ether synthesis using chloro-heterocycles , 2006 .
[24] S. Ahn,et al. Molecular design, synthesis, and hypoglycemic and hypolipidemic activities of novel pyrimidine derivatives having thiazolidinedione. , 2005, European journal of medicinal chemistry.
[25] M. Nieger,et al. A versatile metathesis reaction for the formation of labile bonds between group 13 and group 15 atoms. , 2003, Angewandte Chemie.
[26] S. Ley,et al. Modern Synthetic Methods for Copper‐Mediated C(aryl) ? O, C(aryl) ? N, and C(aryl) ? S Bond Formation , 2003 .
[27] S. Buchwald,et al. Copper-catalyzed coupling of aryl iodides with aliphatic alcohols. , 2002, Organic letters.
[28] D. Venkataraman,et al. Formation of aryl-nitrogen, aryl-oxygen, and aryl-carbon bonds using well-defined copper(I)-based catalysts. , 2001, Organic letters.
[29] J. S. Sawyer. Recent Advances in Diaryl Ether Synthesis , 2000 .
[30] Paul J. Fagan,et al. Using Intelligent/Random Library Screening To Design Focused Libraries for the Optimization of Homogeneous Catalysts: Ullmann Ether Formation , 2000 .
[31] F. Theil,et al. Synthesis of Diaryl Ethers: A Long-Standing Problem Has Been Solved. , 1999, Angewandte Chemie.
[32] S. Buchwald,et al. A GENERAL COPPER-CATALYZED SYNTHESIS OF DIARYL ETHERS , 1997 .
[33] Robert C. Belloli. The misuse of the circle notation to represent aromatic rings , 1983 .
[34] Surajit Sinha,et al. Purmorphamine activates the Hedgehog pathway by targeting Smoothened , 2006, Nature chemical biology.
[35] F. Ullmann. Ueber eine neue Darstellungsweise von Phenyläthersalicylsäure , 1904 .