Catalyst and solvent-free, ultrasound promoted rapid protocol for the one-pot synthesis of α-aminophosphonates at room temperature

[1]  T. Srinivasan,et al.  Choline chloride·2ZnCl2 ionic liquid: an efficient and reusable catalyst for the solvent free Kabachnik–Fields reaction , 2012 .

[2]  C. N. Raju,et al.  Ultrasound‐Assisted Synthesis of Novel α‐Aminophosphonates and Their Biological Activity , 2012, Archiv der Pharmazie.

[3]  Y. Jeong,et al.  Cd(ClO4)2∙xH2O as a novel catalyst for the synthesis of α-aminophosphonates under solvent-free conditions , 2012 .

[4]  C. S. Reddy,et al.  Polyethylene glycol in water: a simple and environment friendly medium for C–P bond formation , 2011 .

[5]  Y. Jeong,et al.  BF3·SiO2-catalyzed one-pot synthesis of α-aminophosphonates in ionic liquid and neat conditions , 2011 .

[6]  J. Nagarkar,et al.  Nano ceria catalyzed synthesis of α-aminophosphonates under ultrasonication , 2011 .

[7]  Pravin V. Shinde,et al.  An organocatalyzed facile and rapid access to α-hydroxy and α-amino phosphonates under conventional/ultrasound technique , 2011 .

[8]  A. Ganesh,et al.  Nano Fe3O4 as magnetically recyclable catalyst for the synthesis of α-aminophosphonates in solvent-free conditions , 2011 .

[9]  A. Fernandes,et al.  MoO2Cl2 as a novel catalyst for the synthesis of α-aminophosphonates , 2011 .

[10]  Zhan‐Hui Zhang,et al.  NbCl5: an efficient catalyst for one‐pot synthesis of α‐aminophosphonates under solvent‐free conditions , 2011 .

[11]  Avelino Corma,et al.  Ceria nanoparticles as heterogeneous catalyst for CO2 fixation by omega-aminoalcohols. , 2010, Chemical communications.

[12]  M. Maghsoodlou,et al.  Al(H2PO4)3 as an Efficient and Reusable Catalyst for One‐pot Three‐component Synthesis of α‐Amino Phosphonates under Solvent‐free Conditions , 2010 .

[13]  M. Abdollahi-Alibeik,et al.  CeCl3·7H2O-catalyzed one-pot Kabachnik–Fields reaction: A green protocol for three-component synthesis of α-aminophosphonates , 2010 .

[14]  A. Vinu,et al.  Mesoporous aluminosilicate nanocage-catalyzed three-component coupling reaction: an expedient synthesis of α-aminophosphonates , 2009 .

[15]  Jin-Ning Dang,et al.  Silica Sulfuric Acid as a Recyclable Catalyst for a One-Pot Synthesis of α-Aminophosphonates in Solvent-Free Conditions , 2009 .

[16]  A. Corma,et al.  Gold nanoparticles promote the catalytic activity of ceria for the transalkylation of propylene carbonate to dimethyl carbonate , 2009 .

[17]  S. Sobhani,et al.  One‐pot synthesis of primary 1‐aminophosphonates: Coupling reaction of carbonyl compounds, hexamethyldisilazane, and diethyl phosphite catalyzed by Al(OTf)3 , 2009 .

[18]  A. Heydari,et al.  A new one-pot synthesis of α-amino phosphonates catalyzed by H3PW12O40 , 2007 .

[19]  C. Stevens,et al.  Synthetic methods for azaheterocyclic phosphonates and their biological activity. , 2004, Chemical reviews.

[20]  S. Chandrasekhar,et al.  Three component coupling catalyzed by TaCl5–SiO2: synthesis of α-amino phosphonates , 2001 .

[21]  J. Yadav,et al.  Zr4+-Catalyzed Efficient Synthesis of α-Aminophosphonates , 2001 .

[22]  S. Shibuya,et al.  Stereoselective Synthesis of .beta.-Oxygenated .alpha.-Hydroxyphosphonates by Lewis Acid-Mediated Stereoselective Hydrophosphonylation of .alpha.-Benzyloxy Aldehydes. An Application to the Synthesis of Phosphonic Acid Analogs of Oxyamino Acids , 1994 .

[23]  R. Chen,et al.  Synthesis and Antitumor Activity of Novel a-Substituted Aminomethylphosphonates , 1994 .

[24]  H. Ha,et al.  An Efficient Synthesis of Anilinobenzylphosphonates , 1992 .

[25]  Paweł Kafarski,et al.  BIOLOGICAL ACTIVITY OF AMINOPHOSPHONIC ACIDS , 1991 .

[26]  L. Maier.  ORGANIC PHOSPHORUS COMPOUNDS 91.1 SYNTHESIS AND PROPERTIES OF 1-AMINO-2-ARYLETHYLPHOSPHONIC AND-PHOSPHINIC ACIDS AS WELL AS -PHOSPHINE OXIDES , 1990 .

[27]  J. Wood,et al.  Renin inhibitors. Synthesis of transition-state analogue inhibitors containing phosphorus acid derivatives at the scissile bond. , 1989, Journal of medicinal chemistry.

[28]  I. A. Natchev.  Synthesis, enzyme — substrate interaction, and herbicidal activity of phosphoryl analogues of glycine , 1988 .

[29]  C. Hassall,et al.  Synthesis and structure-activity relationships of antibacterial phosphonopeptides incorporating (1-aminoethyl)phosphonic acid and (aminomethyl)phosphonic acid. , 1986, Journal of medicinal chemistry.

[30]  J. Craig,et al.  Potential antimalarials. 7. Tribromomethylquinolines and positive halogen compounds. , 1971, Journal of medicinal chemistry.