ZrCl4-Catalyzed Efficient Synthesis of Enaminones and Enamino Esters under Solvent-free Conditions

[1]  R. Bhosale,et al.  Ionic liquid promoted synthesis of β-enamino ketones at room temperature , 2006 .

[2]  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 .

[3]  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 .

[4]  A. Morel,et al.  The solvent free preparation of beta-amino esters alpha,beta-unsaturated ketones and esters with domestic microwave oven , 2006 .

[5]  Li-Ming Song,et al.  A solvent-free synthesis of β-amino-α,β-unsaturated ketones and esters catalysed by sulfated zirconia , 2005 .

[6]  N. Barua,et al.  Iodine‐Catalyzed Conversion of β‐Dicarbonyl Compounds into β‐Enaminones Within a Minute Under Solvent‐Free Conditions , 2005 .

[7]  Yong-mei Wang,et al.  An Efficient and Practical Process for the Synthesis of Bis(indolyl)methanes Catalyzed by Zirconium Tetrachloride , 2005 .

[8]  C. Cimarelli,et al.  The reaction of β-enaminoesters with organolithium reagents: a convenient method for the regioselective synthesis of enaminoketones , 2004 .

[9]  Yuan Gao,et al.  A Convenient and Effective Method for Synthesizing β‐Amino‐α,β‐Unsaturated Esters and Ketones , 2004 .

[10]  C. B. Koning,et al.  Reformatsky reactions with N-arylpyrrolidine-2-thiones: synthesis of tricyclic analogues of quinolone antibacterial agents , 2001 .

[11]  S. Fustero,et al.  N-Substituted β-Enamino Acid Derivatives: A New Approach to Fluorinated β-Enamino Esters , 1997 .

[12]  G. Bartoli,et al.  A versatile route to β-enamino esters by acylation of lithium enamines with diethyl carbonate or benzyl chloroformate , 1995 .

[13]  J. D'angelo,et al.  New chiral auxiliaries: their use in the asymmetric hydrogenation of .beta.-acetamidocrotonates , 1990 .

[14]  D. Boger,et al.  Total synthesis and evaluation of (.+-.)-N-(tert-butoxycarbonyl)-CBI, (.+-.)-CBI-CDPI1, and (.+-.)-CBI-CDPI2: CC-1065 functional agents incorporating the equivalent 1,2,9,9a-tetrahydrocyclopropa[1,2-c]benz[1,2-e]indol-4-one (CBI) left-hand subunit , 1989 .

[15]  A. Saeed Preparation and molecular structure of new cyclic .beta.-diketone Schiff bases , 1984 .

[16]  S. Hannick,et al.  An improved procedure for the Blaise reaction: a short, practical route to the key intermediates of the saxitoxin synthesis , 1983 .

[17]  S. Manfredini,et al.  An Improved Preparation of Enaminones from 1,3-Diketones and Ammonium Acetate or Amine Acetates , 1983 .

[18]  M. Ohno,et al.  Stereocontrolled synthesis of (+)-negamycin from an acyclic homoallylamine by 1,3-asymmetric induction , 1982 .

[19]  R. Sachleben,et al.  Synthetic approach to bicyclomycim: Synthesis of the bicyclic system of bicyclomycin , 1981 .