Silver nanoparticles as an efficient, heterogeneous and recyclable catalyst for synthesis of β-enaminones

[1]  Liang Han,et al.  Efficient synthesis of β-enaminoesters via highly stereoselective Reformatsky reaction with disubstituted formamides as novel electrophiles , 2009 .

[2]  D. Russowsky,et al.  Studies on the Eschenmoser coupling reaction and insights on its mechanism. Application in the synthesis of Norallosedamine and other alkaloids , 2009 .

[3]  E. Rafiee,et al.  CATALYTIC ACTIVITY OF TUNGSTOPHOSPHORIC ACID SUPPORTED ON CARRIERS OF DIVERSE ACIDITY IN THE SYNTHESIS OF ENAMINONES , 2009 .

[4]  A. Murugadoss,et al.  Surface Area Controlled Differential Catalytic Activities of One-Dimensional Chain-like Arrays of Gold Nanoparticles , 2008 .

[5]  S. Ghosh,et al.  The antibacterial properties of a novel chitosan-Ag-nanoparticle composite. , 2008, International journal of food microbiology.

[6]  A. Murugadoss,et al.  A ‘green’ chitosan–silver nanoparticle composite as a heterogeneous as well as micro-heterogeneous catalyst , 2008, Nanotechnology.

[7]  K. Watson,et al.  Total synthesis of anibamine, a novel natural product as a chemokine receptor CCR5 antagonist. , 2007, Organic letters.

[8]  S. Genovese,et al.  “Ytterbium triflate catalyzed synthesis of β-enaminones”, , 2007 .

[9]  Zhan‐Hui Zhang,et al.  Cobalt(II) chloride-mediated synthesis of beta-enamino compounds under solvent-free conditions , 2006 .

[10]  Li Lin,et al.  A novel, practical and green synthesis of Ag nanoparticles catalyst and its application in three-component coupling of aldehyde, alkyne, and amine , 2006 .

[11]  C. Cimarelli,et al.  Chemo- and Stereoselective Reduction of Enaminones for the Preparation of Biologically Active Compounds , 2006 .

[12]  Y. K. Rao,et al.  Highly efficient, mild and chemo- and stereoselective synthesis of enaminones and enamino esters using silica supported perchloric acid under solvent-free conditions , 2006 .

[13]  D. Ihle,et al.  Tandem photocycloaddition-retro-mannich fragmentation of enaminones. A route to spiropyrrolines and the tetracyclic core of koumine. , 2006, Organic letters.

[14]  K. Srinivasan,et al.  A remarkably rapid regioselective synthesis of β-enaminones using silica chloride in a heterogeneous as well as an ionic liquid in a homogeneous medium at room temperature , 2006 .

[15]  Yong-mei Wang,et al.  A General and Efficient Method for the Preparation of β-Enamino Ketones and Esters Catalyzed by Indium Tribromide , 2006 .

[16]  Feng Lu,et al.  Nanoparticles as recyclable catalysts: the frontier between homogeneous and heterogeneous catalysis. , 2005, Angewandte Chemie.

[17]  M. Abass,et al.  Synthesis and evaluation of molluscicidal and larvicidal activities of some novel enaminones derived from 4-hydroxyquinolinones: part IX. , 2005, Bioorganic & medicinal chemistry.

[18]  Hongbin Zhang,et al.  Efficient synthesis of -amino-a,-unsaturated carbonyl compounds , 2005 .

[19]  C. Brandt,et al.  Efficient Synthetic Method for β-Enamino Esters Using Ultrasound , 2004 .

[20]  D. Russowsky,et al.  A concise and stereoselective synthesis of (+/)-erythro-methylphenidate , 2003 .

[21]  Matthew T. Epperson,et al.  Enantiospecific synthesis of the bridged pyrrolizidine core of asparagamine A: dipolar cycloadditions of azomethine ylides derived from the sulfonylation of vinylogous amides. , 2002, Angewandte Chemie.

[22]  J. Stables,et al.  Enaminones-versatile therapeutic pharmacophores. Further advances. , 2000, Current medicinal chemistry.

[23]  J. Hamelin,et al.  Synthesis in dry media coupled with microwave irradiation : Application to the preparation of enaminoketones. , 1993 .