Gold complex-catalyzed CP bond formation by Kabachnik–Fields reactions

[1]  Le‐Ping Liu,et al.  Recent advances in the isolation and reactivity of organogold complexes. , 2012, Chemical Society reviews.

[2]  G. Hammond,et al.  Ligand effects and ligand design in homogeneous gold(I) catalysis. , 2012, Journal of the American Chemical Society.

[3]  Z. Pászti,et al.  Gold Catalysis: Effect of Particle Size on Reactivity Towards Various Substrates , 2012 .

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

[5]  E. Wagner,et al.  Hydrogen Bonding in α-Aminophosphonic Acids , 2012 .

[6]  K. Yoon,et al.  Zn(OAc)2•2H2O‐catalyzed synthesis of α‐aminophosphonates under neat reaction , 2012 .

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

[8]  A. Gee,et al.  Au(I) /Au(III) catalysis: an alternative approach for C-C oxidative coupling. , 2011, Chemistry.

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

[10]  Francisco J. Sayago,et al.  Stereodivergent Synthesis of Two Novel α-Aminophosphonic Acids Characterised by a cis-Fused Octahydroindole System , 2011 .

[11]  A. Schuster,et al.  Gold catalysis: 1,3-oxazines by cyclisation of allene amides. , 2011, Chemistry.

[12]  Raquel P. Herrera,et al.  Thiourea catalyzed organocatalytic enantioselective Michael addition of diphenyl phosphite to nitroalkenes. , 2011, Organic & biomolecular chemistry.

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

[14]  Yixiang Cheng,et al.  Gold-complexes catalyzed oxidative α-cyanation of tertiary amines. , 2011, Chemical communications.

[15]  Limin Wang,et al.  A facile synthesis of α-aminophosphonates catalyzed by ytterbium perfluorooctanoate under solvent-free conditions , 2011 .

[16]  K. Ando,et al.  Facile synthesis of α‐amino phosphonates in water by Kabachnik–Fields reaction using magnesium dodecyl sulfate , 2011 .

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

[18]  B. Banik,et al.  A Highly Efficient Bismuth Salts-Catalyzed Route for the Synthesis of α-Aminophosphonates , 2010, Molecules.

[19]  M. Maghsoodlou,et al.  Silica Supported Perchloric Acid (HClO4 – SiO2): Highly Efficient Heterogeneous Catalyst for the Synthesis of α-Amino Phosphonates , 2010 .

[20]  S. Raghavan,et al.  Synthesis, Characterization and Evaluation of Cytotoxicity of New Aminophosphonic Acid Diesters in Human Leukemia Cells , 2010 .

[21]  A. Shirazi,et al.  Silica gel and polystyrene supported aluminum chloride as heterogeneous catalysts for the preparation of α‐aminophosphonates , 2010 .

[22]  M. Sieńczyk,et al.  Irreversible inhibition of serine proteases - design and in vivo activity of diaryl alpha-aminophosphonate derivatives. , 2009, Current medicinal chemistry.

[23]  P. Kafarski,et al.  Biological Activity of Aminophosphonic Acids and Their Short Peptides , 2009 .

[24]  M. Gdaniec,et al.  Synthesis and structure of products of interaction of H[AuCl4] with H2DMG and pyridine , 2007 .

[25]  A. Rheingold,et al.  Gold(III) and platinum(II) polypyridyl double salts and a general metathesis route to metallophilic interactions. , 2006, Inorganic chemistry.

[26]  A. Hashmi,et al.  Gold catalysis: the benefits of N and N,O ligands. , 2004, Angewandte Chemie.

[27]  A. Manjula,et al.  One-Pot Synthesis of α-Aminophosphonates: An Inexpensive Approach , 2003 .

[28]  B. Kaboudin.  A convenient synthesis of 1-aminophosphonates from 1-hydroxyphosphonates , 2003 .

[29]  A. Zwierzak,et al.  An expeditious one-pot synthesis of diethyl N-Boc-1-aminoalkylphosphonates , 2002 .

[30]  A. Lützen,et al.  Diastereoselective Lewis acid mediated hydrophosphonylation of heterocyclic imines: a stereoselective approach towards α-amino phosphonates , 2001 .

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

[32]  A. Hashmi,et al.  A New Gold-Catalyzed C—C Bond Formation. , 2000 .

[33]  I. Gancarz,et al.  Nucleophilic addition to carbonyl compounds. competition between hard (amine) and soft (phosphite) nucleophile , 1995 .

[34]  S. Laschat,et al.  Carbohydrates as Chiral Templates: Stereoselective Synthesis of (R)- and (S)-α-Aminophosphonic Acid Derivatives , 1992 .