Synthesis of Biginelli adducts using a Preyssler heteropolyacid in silica matrix from biomass building block

[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 .