Efficient conversion of aldehydes and ketones into oximes using a nanostructured pyrophosphate catalyst in a solvent-free process
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[1] Pingle Liu,et al. Hydrogenation of nitrocyclohexane to cyclohexanone oxime over Pd/CNT catalyst under mild conditions , 2012 .
[2] Rafael Luque,et al. Magnetically recoverable nanocatalysts. , 2011, Chemical reviews.
[3] M. Bousmina,et al. Clean chemical synthesis of 2-amino-chromenes in water catalyzed by nanostructured diphosphate Na2CaP2O7 , 2010 .
[4] Rajender S. Varma,et al. Green chemistry by nano-catalysis , 2010 .
[5] M. El-Gamal,et al. Synthesis and anti-inflammatory activity of novel (substituted)benzylidene acetone oxime ether derivatives: molecular modeling study. , 2010, European journal of medicinal chemistry.
[6] Y. Li,et al. A Concise, Metal-Free Approach to the Synthesis of Oxime Ethers from Cross-Dehydrogenative-Coupling of sp3 C-H Bonds with Oximes , 2010 .
[7] Y. Jeong,et al. Stereospecific synthesis of oximes and oxime ethers of 3-azabicycles: A SAR study towards antimicrobial agents. , 2010, Bioorganic & medicinal chemistry letters.
[8] A. Padwa,et al. 2,3-Bis(phenylsulfonyl)-1,3-butadiene as a reagent for the synthesis of the azatricyclic core of (+/-)-halichlorine. , 2010, The Journal of organic chemistry.
[9] S. Nolan,et al. Au/Ag-cocatalyzed aldoximes to amides rearrangement under solvent- and acid-free conditions. , 2010, The Journal of organic chemistry.
[10] Paul Anastas,et al. Green chemistry: principles and practice. , 2010, Chemical Society reviews.
[11] V. Rives,et al. Synthesis of paracetamol by liquid phase Beckmann rearrangement of 4-hydroxyacetophenone oxime over H3PO4/Al-MCM-41 , 2009 .
[12] B. Cheng,et al. Ultrasound-promoted synthesis of oximes catalyzed by a basic ionic liquid [bmIm]OH. , 2009, Ultrasonics sonochemistry.
[13] C. Kappe,et al. Practical Microwave Synthesis for Organic Chemists: Strategies, Instruments, and Protocols , 2009 .
[14] H. Mehrabi. Synthesis of α-oximinoketones under ultrasound irradiation , 2008 .
[15] C. Kappe,et al. Microwave-assisted synthesis in water as solvent. , 2007, Chemical reviews.
[16] Ji-tai Li,et al. Synthesis of oximes under ultrasound irradiation. , 2006, Ultrasonics sonochemistry.
[17] I. Damljanović,et al. A Simple Synthesis of Oximes , 2006 .
[18] H. Eshghi,et al. REGIOSELECTIVE SYNTHESIS OF E-OXIMES CATALYZED BY FERRIC CHLORIDE UNDER SOLVENT-FREE CONDITIONS , 2005 .
[19] Wen-jie Zheng,et al. A Novel Ionic Liquid/water Biphasic System for the Preparation of Oximes , 2005 .
[20] Gabor A. Somorjai,et al. High technology catalysts towards 100% selectivity: Fabrication, characterization and reaction studies , 2005 .
[21] S. Sebti,et al. Na2CaP2O7, a new catalyst for the synthesis of unsaturated arylsulfones , 2003 .
[22] E. Lukevics,,et al. Indole and Isatin Oximes: Synthesis, Reactions, and Biological Activity. (Review) , 2003 .
[23] M. White,et al. Recent advances in nanocatalysis research , 2002 .
[24] A. Tomilov,et al. Phase-Transfer Catalysis in Synthesis of Oximes , 2002 .
[25] Jasvinder Singh,et al. Solventless preparation of oximes in the solid state and via microwave irradiation , 2001 .
[26] W. Ou,et al. Preparation of cyclic ketoximes using aqueous hydroxylamine in ionic liquids , 2001 .
[27] J. Ley,et al. Hydroxy- or methoxy-substituted benzaldoximes and benzaldehyde-O-alkyloximes as tyrosinase inhibitors. , 2001, Bioorganic & medicinal chemistry.
[28] A. Hallberg,et al. Microwave-assisted high-speed chemistry: a new technique in drug discovery. , 2001, Drug discovery today.
[29] Tong‐Shuang Li,et al. TiO2/SO42−: an efficient and convenient catalyst for preparation of aromatic oximes , 2001 .
[30] H. Sharghi,et al. A Mild and Versatile Method for the Preparation of Oximes by Use of Calcium Oxide † , 2000 .
[31] E. M. Holt,et al. Synthesis and crystal structure of Na2CaP2O7 , 1999 .
[32] A. Pombeiro,et al. Oxime and oximate metal complexes: unconventional synthesis and reactivity , 1999 .
[33] A. Hajipour,et al. 1-BENZYL-4-AZA-1-AZONIABICYCLO[2.2.2]OCTANE PERIODATE: A MILD AND EFFICIENT OXIDANT FOR THE CLEAVAGE OF OXIME DOUBLE BONDS UNDER ANHYDROUS CONDITIONS , 1998 .
[34] R. Ballini,et al. Amberlyst A-21 an Excellent Heterogeneous Catalyst for the Conversion of Carbonyl Compounds to Oximes , 1997 .
[35] Arun S. Mujumdar,et al. Introduction to Surface Chemistry and Catalysis , 1994 .
[36] D. Sigman,et al. New inhibitors of aldose reductase: anti-oximes of aromatic aldehydes. , 1991, Archives of biochemistry and biophysics.
[37] G. Sosnovsky,et al. A One-Flask Conversion of Aldehydes to Nitriles Using Hydroxylamine Hydrochloride and Selenium Dioxide , 1979 .
[38] G. Olah,et al. Synthetic Methods and Reactions; 601. Improved One-Step Conversion of Aldehydes into Nitriles with Hydroxylamine in Formic Acid Solution , 1979 .