Significant rate acceleration of the aza-Michael reaction in water

[1]  Gopal L. Khatik,et al.  Catalyst-Free Conjugated Addition of Thiols to α,β-Unsaturated Carbonyl Compounds in Water , 2006 .

[2]  K. R. Rao,et al.  β-Cyclodextrin promoted aza-Michael addition of amines to conjugated alkenes in water , 2006 .

[3]  M. R. Saidi,et al.  One-pot synthesis of dithiocarbamates accelerated in water. , 2006, The Journal of organic chemistry.

[4]  Sahid Hussain,et al.  Boric acid: a novel and safe catalyst for aza-Michael reactions in water , 2005 .

[5]  J. Collin,et al.  Aza-Michael reactions catalyzed by samarium diiodide , 2005 .

[6]  A. Verma,et al.  Cu-nanoparticles: a chemoselective catalyst for the aza-Michael reactions of N-alkyl- and N-arylpiperazines with acrylonitrile , 2005 .

[7]  M. R. Saidi,et al.  Highly chemoselective addition of amines to epoxides in water. , 2005, Organic letters.

[8]  Lei Yang,et al.  Highly efficient KF/Al2O3-catalyzed versatile hetero-Michael addition of nitrogen, oxygen, and sulfur nucleophiles to α,β-ethylenic compounds , 2005 .

[9]  Sahid Hussain,et al.  Cu(acac)2 Immobilized in Ionic Liquids: A Recoverable and Reusable Catalytic System for Aza‐Michael Reactions , 2005 .

[10]  P. Das,et al.  Synthesis of β-amino esters via aza-michael addition of amines to alkenes promoted on silica: A useful and recyclable surface , 2004 .

[11]  Shaolin Zhou,et al.  A green, ionic liquid and quaternary ammonium salt-catalyzed aza-Michael reaction of α,β-ethylenic compounds with amines in water , 2004 .

[12]  N. Azizi,et al.  LiClO4 Accelerated Michael addition of amines to α,β-unsaturated olefins under solvent-free conditions , 2004 .

[13]  B. Ranu,et al.  Solvent-free, catalyst-free Michael-type addition of amines to electron-deficient alkenes , 2002 .

[14]  J. Spencer,et al.  Convenient synthesis of Cbz-protected β-amino ketones by a copper-catalysed conjugate addition reaction , 2002 .

[15]  E. Marcantoni,et al.  Conjugate Addition of Amines to α,β-Enones Promoted by CeCl3·7H2O−NaI System Supported in Silica Gel , 2001 .

[16]  T. Loh,et al.  Indium Trichloride-Catalyzed Conjugate Addition of Amines to α,β-Ethylenic Compounds in Water , 1998 .

[17]  M. Sodeoka,et al.  Enantioselective Addition of Enol Silyl Ethers to Imines Catalyzed by Palladium Complexes: A Novel Way to Optically Active Acylalanine Derivatives , 1998 .

[18]  P. Grieco Organic synthesis in water , 1998 .

[19]  Chao-Jun Li,et al.  Organic reactions in aqueous media , 1997 .

[20]  E. Corey,et al.  A Novel Chiral Super-Lewis Acidic Catalyst for Enantioselective Synthesis , 1996 .

[21]  C. Tomasini,et al.  Asymmetric synthesis of ß-amino acids and α-substituted β-amino acids , 1996 .

[22]  G. Jenner Catalytic high pressure synthesis of hindered β-aminoesters , 1995 .

[23]  E. Marcantoni,et al.  Chemo- and Diastereoselective Reduction of .beta.-Enamino Esters: A Convenient Synthesis of Both cis- and trans-.gamma.-Amino Alcohols and .beta.-Amino Esters , 1994 .

[24]  S. Matsubara,et al.  Lanthanoid Triflate Catalyzed Conjugate Addition of Amines to α, β-Unsaturated Esters. A Facile Route to Optically Active β-Lactam , 1994 .

[25]  P. Laszlo,et al.  Catalysis of the specific michael addition : The example of acrylate acceptors , 1989 .

[26]  R. Crouch,et al.  The Condensation of Oxalic Esters with Esters of β-Alanine and N-Substituted β-Aminopropionic Acids. Synthesis of Some Derivatives of 2,3-Dioxopyrrolidine and 2-Oxo-3-methoxy-3-pyrroline , 1953 .