Synthesis of Biginelli adducts using a Preyssler heteropolyacid in silica matrix from biomass building block
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G. Romanelli | T. Rezende | S. A. Fernandes | Á. Sathicq | José J. Martínez | Omar M. Portilla-Zuñiga | S. Fernandes | Omar Portilla-Zúñiga
[1] T. Constantieux,et al. Preyssler Heteropoly Acids Encapsulated in a Silica Framework for an Efficient Preparation of Fluorinated Hexahydropyrimidine Derivatives under Solvent-Free Conditions , 2014, Synlett.
[2] M. Nasr-Esfahani,et al. EFFICIENT AND GREEN CATALYTIC SYNTHESIS OF DIHYDROPYRIMIDINONE (THIONE) DERIVATIVES USING COBALT NITRATE IN SOLVENT-FREE CONDITIONS , 2014 .
[3] S. Ramakrishna,et al. Modified Biginelli reaction: Synthesis of fused Dihydropyrimidones , 2014 .
[4] R. Luque,et al. Solvent-free and catalysts-free chemistry: a benign pathway to sustainability. , 2014, ChemSusChem.
[5] Xufeng Lin,et al. Efficient synthesis of dihydropyrimidinones via a three-component Biginelli-type reaction of urea, alkylaldehyde and arylaldehyde , 2013, Beilstein journal of organic chemistry.
[6] J. Esperança,et al. Direct transformation of 5-hydroxymethylfurfural to the building blocks 2,5-dihydroxymethylfurfural (DHMF) and 5-hydroxymethyl furanoic acid (HMFA) via Cannizzaro reaction , 2013 .
[7] S. Sajjadifar,et al. Novel acidic ionic liquid as a catalyst and solvent for green synthesis of dihydropyrimidine derivatives , 2013 .
[8] Shubha Jain,et al. Green protocol for the synthesis of 3,4-Dihydropyrimidin-2(1H)- ones/thiones using TBAB as a catalyst and solvent free condition under microwave irradiation , 2012 .
[9] C. Afonso,et al. 5-Hydroxymethylfurfural (HMF) as a building block platform: Biological properties, synthesis and synthetic applications , 2011 .
[10] Xi‐Cun Wang,et al. PS–PEG–SO3H as an efficient catalyst for 3,4-dihydropyrimidones via Biginelli reaction , 2009 .
[11] V. Mamedov,et al. New potential of the classical Biginelli reaction , 2008 .
[12] Heng Jiang,et al. An Efficient One‐Pot Biginelli Condensation of Aliphatic Aldehydes Catalyzed by Zinc Bromide under Solvent‐Free Conditions , 2007, Preparative biochemistry & biotechnology.
[13] D. Vos,et al. Furfural and Derivatives , 2007 .
[14] M. T. Pope,et al. The Sodium Pentaphosphato(V)‐Triacontatungstate Anion Isolated as the Ammonium Salt , 2007 .
[15] S. Tangestaninejad,et al. One-pot synthesis of dihydropyrimidinones using facile and reusable polyoxometalate catalysts for the Biginelli reaction , 2006 .
[16] F. Bamoharram,et al. Preyssler catalyst,[NaP5W30O110](14-) : A green, efficient and reusable catalyst for esterification of salicylic acid with aliphatic and benzylic alcohols , 2006 .
[17] Jomy Joseph,et al. Ion exchange resins as recyclable and heterogeneous solid acid catalysts for the Biginelli condensation : An improved protocol for the synthesis of 3,4-dihydropyrimidin-2-ones , 2006 .
[18] V. Nair. Multicomponent Reactions. Edited by Jieping Zhu and Hugues Bienyamé. , 2005 .
[19] S. Pednekar,et al. Large scale Biginelli reaction via water-based biphasic media: a green chemistry strategy , 2005 .
[20] Sanjay W. Chavhan,et al. New environmentally benign protocol for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones: Practical access to mitotic kinesin EG5 inhibitor Monastrol , 2005 .
[21] C. Kappe,et al. The Biginelli Dihydropyrimidine Synthesis , 2004 .
[22] A. Sudalai,et al. Cu(OTf)2: a reusable catalyst for high-yield synthesis of 3,4-dihydropyrimidin-2(1H)-ones , 2003 .
[23] Shan-Wei Wang,et al. Indium(III) bromide-catalyzed preparation of dihydropyrimidinones: improved protocol conditions for the Biginelli reaction , 2002 .
[24] M. Mahesh,et al. Zirconium(IV) chloride catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones☆ , 2002 .
[25] C. S. Reddy,et al. ChemInform Abstract: Mn(OAc)3×2H2O-Mediated Three-Component, One-Pot Condensation Reaction: An Efficient Synthesis of 4-Aryl-Substituted 3,4-Dihydropyrimidin-2-ones. , 2001 .
[26] J. Yadav,et al. Ultrasound-accelerated synthesis of 3,4-dihydropyrimidin-2(1H)-ones with ceric ammonium nitrate , 2001 .
[27] Zi-Yang Zhang,et al. An Efficient Synthesis of 5-Alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones Catalyzed by KSF Montmorillonite , 2000 .
[28] B. Ranu,et al. Indium(III) chloride-catalyzed one-pot synthesis of dihydropyrimidinones by a three-component coupling of 1,3-dicarbonyl compounds, aldehydes, and urea: an improved procedure for the Biginelli reaction. , 2000, The Journal of organic chemistry.
[29] McDonnell,et al. A new substrate for the Biginelli cyclocondensation: direct preparation of 5-unsubstituted 3,4-dihydropyrimidin-2(1H)-ones from a beta-keto carboxylic acid , 2000, The Journal of organic chemistry.
[30] C. Qian,et al. Lanthanide triflate catalyzed Biginelli reaction. one-pot synthesis of dihydropyrimidinones under solvent-free conditions. , 2000, The Journal of organic chemistry.
[31] C. Kappe,et al. Design and Synthesis of a Conformationally Rigid Mimic of the Dihydropyrimidine Calcium Channel Modulator SQ 32,926 , 2000 .
[32] A. Lubineau,et al. Water as Solvent in Organic Synthesis , 1999 .
[33] C. Kappe. A Reexamination of the Mechanism of the Biginelli Dihydropyrimidine Synthesis. Support for an N-Acyliminium Ion Intermediate(1). , 1997, The Journal of organic chemistry.
[34] M. Malley,et al. Synthesis of substituted 1,2,3,4-tetrahydro-6-methyl-2-thioxo-5-pyrimidinecarboxylic acid esters , 1987 .
[35] P. Biginelli. Ueber Aldehyduramide des Acetessigäthers , 1891 .