Pumice as a Novel Natural Heterogeneous Catalyst for the Designation of 3,4-Dihydropyrimidine-2-(1H)-ones/thiones under Solvent-Free Conditions
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A. A. Abdelhamid | M. M. Khalaf | M. Gouda | S. Shaaban | H. M. El-Lateef | Nadia A. A. Elkanzi | Ali M. Ali | El Sayed A. Saber
[1] A. A. Abdelhamid,et al. Microwave-Assisted, One-Pot Multicomponent Synthesis of Some New Cyanopyridines , 2017 .
[2] Ali M. Ali,et al. Synthesis of Novel Chromene, Pyridine, Pyrazole, Pyrimidine, and Imidazole Derivatives via One‐pot Multicomponent Reaction , 2017 .
[3] S. Bahekar,et al. Simple and efficient synthesis of 3,4-dihydropyrimidin-2(1H)-thiones utilizing l-proline nitrate as a proficient, recyclable and eco-friendly catalyst , 2017 .
[4] S. Boukhris,et al. EASY SYNTHESIS OF 3,4-DIHYDROPYRIMIDIN -2-(1H)-ONES USING PHOSPHATE FERTILIZERS MAP, DAP AND TSP AS EFFICIENT CATALYSTS , 2017 .
[5] A. A. Abdelhamid,et al. Multicomponent Green Synthesis, Spectroscopic and Structural Investigation of Multi‐Substituted Imidazoles. Part 1. , 2016 .
[6] A. A. Abdelhamid,et al. Sol–gel Derived Mixed Oxide Zirconia: Titania Green Heterogeneous Catalysts and Their Performance in Acridine Derivatives Synthesis , 2016, Catalysis Letters.
[7] A. A. Abdelhamid,et al. Multicomponent green synthesis, spectroscopic and structural investigation of multi-substituted imidazoles. Part 1 , 2015 .
[8] A. E. Manawi,et al. Volcano-sedimentary characteristics in the Abu Treifiya Basin, Cairo–Suez District, Egypt: Example of dynamics and fluidization over sedimentary and volcaniclastic beds by emplacement of syn-volcanic basaltic rocks , 2015 .
[9] David R. Cole,et al. Characterization and Analysis of Porosity and Pore Structures , 2015 .
[10] P. Barman,et al. Grindstone chemistry: a highly efficient and green method for synthesis of 3,4-dihydropyrimidin-2-(1H)-ones by L-tyrosine as an organocatalyst: a combined experimental and DFT study , 2014 .
[11] F. Shirini,et al. N‐Sulfonic Acid Poly(4‐vinylpyridinium) Chloride as a Highly Efficient and Reusable Catalyst for the Biginelli Reaction. , 2014 .
[12] J. Safari,et al. Carbon nanotubes supported by titanium dioxide nanoparticles as recyclable and green catalyst for mild synthesis of dihydropyrimidinones/thiones , 2014 .
[13] G. Rao,et al. An Efficient Synthesis of β‐Ketoesters via Transesterification and Its Application in Biginelli Reaction under Solvent‐Free, Catalyst‐Free Conditions. , 2014 .
[14] T. Depci,et al. Effect of physical, chemical and electro-kinetic properties of pumice samples on radiation shielding properties of pumice material , 2014 .
[15] Shubha Jain,et al. Silica-bonded N-propyl sulfamic acid as an efficient recyclable catalyst for the synthesis of 3,4-dihydropyrimidin-2-(1H)-ones/thiones under heterogeneous conditions , 2014 .
[16] F. Shirini,et al. N-Sulfonic acid poly(4-vinylpyridinium) chloride as a highly efficient and reusable catalyst for the Biginelli reaction , 2014 .
[17] G. Rao,et al. An efficient synthesis of β-ketoesters via transesterification and its application in Biginelli reaction under solvent-free, catalyst-free conditions , 2013 .
[18] Hamid Reza Ghaffari,et al. Removal of hardness agents, calcium and magnesium, by natural and alkaline modified pumice stones in single and binary systems , 2013 .
[19] F. Atabi,et al. Porosity, characterization and structural properties of natural zeolite - clinoptilolite - as a sorbent , 2013 .
[20] A. Dadhania,et al. A facile approach for the synthesis of 3,4-dihydropyrimidin-2-(1H)-ones using a microwave promoted Biginelli protocol in ionic liquid , 2012, Journal of Chemical Sciences.
[21] G. Christidis,et al. Zeolite Formation and Deposits , 2012 .
[22] S. Patil,et al. Pineapple Juice as a Natural Catalyst: An Excellent Catalyst for Biginelli Reaction , 2011 .
[23] Sanjeev K. Verma,et al. N,N′‐Dichlorobis(2,4,6‐trichlorophenyl)urea (CC‐2) as a New Reagent for the Synthesis of Pyrimidone and Pyrimidine Derivatives via Biginelli Reaction. , 2011 .
[24] A. A. Abdelhamid,et al. 9-(5-Bromo-2-hydroxyphenyl)-10-(2-hydroxypropyl)-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione , 2011, Acta crystallographica. Section E, Structure reports online.
[25] Sanjeev K. Verma,et al. N,N′-Dichlorobis(2,4,6-trichlorophenyl)urea (CC-2) as a new reagent for the synthesis of pyrimidone and pyrimidine derivatives via Biginelli reaction , 2011 .
[26] Q. Huo. Synthetic Chemistry of the Inorganic Ordered Porous Materials , 2011 .
[27] R. Borah,et al. A new protocol for Biginelli (or like) reaction under solvent-free grinding method using Fe (NO3)3.9H2O as catalyst , 2010 .
[28] Xinxiang Luo,et al. New observation on a class of old reactions: Chemoselectivity for the solvent-free reaction of aromatic aldehydes with alkylketones catalyzed by a double-component inorganic base system , 2010 .
[29] A. Jafari,et al. Synthesis of 3,4-dihydropyrimidin-2(1H)-ones and 1,4-dihydropyridines using ammonium carbonate in water , 2010 .
[30] C. Bolm,et al. Organocatalytic reactions: effects of ball milling, microwave and ultrasound irradiation , 2008 .
[31] H. Adibi,et al. Iron(III) trifluoroacetate and trifluoromethanesulfonate: Recyclable Lewis acid catalysts for one-pot synthesis of 3,4-dihydropyrimidinones or their sulfur analogues and 1,4-dihydropyridines via solvent-free Biginelli and Hantzsch condensation protocols , 2007 .
[32] I. Cepanec,et al. Antimony(III) chloride-catalysed Biginelli reaction : a versatile method for the synthesis of dihydropyrimidinones through a different reaction mechanism , 2007 .
[33] C. Bolm,et al. Solvent-Free Carbon-Carbon Bond Formations in Ball Mills , 2007 .
[34] Henk van Koningsveld,et al. Compendium of Zeolite Framework Types: Building Schemes and Type Characteristics , 2007 .
[35] J. Bazureau,et al. Acidic task-specific ionic liquid as catalyst of microwave-assisted solvent-free Biginelli reaction , 2007 .
[36] W. Su,et al. One-pot synthesis of dihydropyrimidiones catalyzed by strontium(II) triflate under solvent-free conditions , 2005 .
[37] K. Nagaiah,et al. A Novel L-Proline Catalyzed Biginelli Reaction : One-Pot Synthesis of 3, 4-Dihydropyrimidin-2(1H)-ones under Solvent-Free Conditions , 2004 .
[38] S. Raddatz,et al. Dihydropyrimidinones--a new class of anti-staphylococcal antibiotics. , 2003, Bioorganic & medicinal chemistry letters.
[39] Jiajian Peng,et al. Ionic liquids catalyzed Biginelli reaction under solvent-free conditions , 2001 .
[40] C. Kappe. Biologically active dihydropyrimidones of the Biginelli-type--a literature survey. , 2000, European journal of medicinal chemistry.
[41] C. Qian,et al. Lanthanide triflate catalyzed Biginelli reaction. one-pot synthesis of dihydropyrimidinones under solvent-free conditions. , 2000, The Journal of organic chemistry.
[42] K. Tanaka,et al. Solvent-free organic synthesis. , 2000, Chemical reviews.
[43] C. Raston,et al. Chemoselective, solvent-free aldol condensation reaction , 2000 .
[44] G. Kaupp,et al. Quantitative solid–solid synthesis of azomethines , 1998 .
[45] A Hedberg,et al. Dihydropyrimidine calcium channel blockers. 3. 3-Carbamoyl-4-aryl-1,2,3,4-tetrahydro-6-methyl-5-pyrimidinecarboxylic acid esters as orally effective antihypertensive agents. , 1991, Journal of medicinal chemistry.
[46] R. W. Le Maitre,et al. A Chemical Classification of Volcanic Rocks Based on the Total Alkali-Silica Diagram , 1986 .
[47] N. Giordano,et al. Hydrothermal synthesis of zeolites from pumice in alkaline and saline environment , 1982 .